The 4th cranial nerve. The trochlear nerve carries the motor innervation of the superior oblique muscles of the eye.
Diseases of the fourth cranial (trochlear) nerve or its nucleus in the midbrain. The nerve crosses as it exits the midbrain dorsally and may be injured along its course through the intracranial space, cavernous sinus, superior orbital fissure, or orbit. Clinical manifestations include weakness of the superior oblique muscle which causes vertical DIPLOPIA that is maximal when the affected eye is adducted and directed inferiorly. Head tilt may be seen as a compensatory mechanism for diplopia and rotation of the visual axis. Common etiologies include CRANIOCEREBRAL TRAUMA and INFRATENTORIAL NEOPLASMS.
Traumatic injuries to the TROCHLEAR NERVE.
Conditions which produce injury or dysfunction of the second cranial or optic nerve, which is generally considered a component of the central nervous system. Damage to optic nerve fibers may occur at or near their origin in the retina, at the optic disk, or in the nerve, optic chiasm, optic tract, or lateral geniculate nuclei. Clinical manifestations may include decreased visual acuity and contrast sensitivity, impaired color vision, and an afferent pupillary defect.
The 6th cranial nerve which originates in the ABDUCENS NUCLEUS of the PONS and sends motor fibers to the lateral rectus muscles of the EYE. Damage to the nerve or its nucleus disrupts horizontal eye movement control.
Diseases of the first cranial (olfactory) nerve, which usually feature anosmia or other alterations in the sense of smell and taste. Anosmia may be associated with NEOPLASMS; CENTRAL NERVOUS SYSTEM INFECTIONS; CRANIOCEREBRAL TRAUMA; inherited conditions; toxins; METABOLIC DISEASES; tobacco abuse; and other conditions. (Adams et al., Principles of Neurology, 6th ed, pp229-31)
Diseases of the tenth cranial nerve, including brain stem lesions involving its nuclei (solitary, ambiguus, and dorsal motor), nerve fascicles, and intracranial and extracranial course. Clinical manifestations may include dysphagia, vocal cord weakness, and alterations of parasympathetic tone in the thorax and abdomen.
Disorders of one or more of the twelve cranial nerves. With the exception of the optic and olfactory nerves, this includes disorders of the brain stem nuclei from which the cranial nerves originate or terminate.
A sensory branch of the trigeminal (5th cranial) nerve. The ophthalmic nerve carries general afferents from the superficial division of the face including the eyeball, conjunctiva, upper eyelid, upper nose, nasal mucosa, and scalp.
A visual symptom in which a single object is perceived by the visual cortex as two objects rather than one. Disorders associated with this condition include REFRACTIVE ERRORS; STRABISMUS; OCULOMOTOR NERVE DISEASES; TROCHLEAR NERVE DISEASES; ABDUCENS NERVE DISEASES; and diseases of the BRAIN STEM and OCCIPITAL LOBE.
Large endothelium-lined venous channels situated between the two layers of DURA MATER, the endosteal and the meningeal layers. They are devoid of valves and are parts of the venous system of dura mater. Major cranial sinuses include a postero-superior group (such as superior sagittal, inferior sagittal, straight, transverse, and occipital) and an antero-inferior group (such as cavernous, petrosal, and basilar plexus).
An idiopathic syndrome characterized by the formation of granulation tissue in the anterior cavernous sinus or superior orbital fissure, producing a painful ophthalmoplegia. (Adams et al., Principles of Neurology, 6th ed, p271)
One of three principal openings in the SUBARACHNOID SPACE. They are also known as cerebellomedullary cistern, and collectively as cisterns.
Paralysis of one or more of the ocular muscles due to disorders of the eye muscles, neuromuscular junction, supporting soft tissue, tendons, or innervation to the muscles.
Diseases of the twelfth cranial (hypoglossal) nerve or nuclei. The nuclei and fascicles of the nerve are located in the medulla, and the nerve exits the skull via the hypoglossal foramen and innervates the muscles of the tongue. Lower brain stem diseases, including ischemia and MOTOR NEURON DISEASES may affect the nuclei or nerve fascicles. The nerve may also be injured by diseases of the posterior fossa or skull base. Clinical manifestations include unilateral weakness of tongue musculature and lingual dysarthria, with deviation of the tongue towards the side of weakness upon attempted protrusion.
The muscles that move the eye. Included in this group are the medial rectus, lateral rectus, superior rectus, inferior rectus, inferior oblique, superior oblique, musculus orbitalis, and levator palpebrae superioris.
Pathological processes of the VESTIBULOCOCHLEAR NERVE, including the branches of COCHLEAR NERVE and VESTIBULAR NERVE. Common examples are VESTIBULAR NEURITIS, cochlear neuritis, and ACOUSTIC NEUROMA. Clinical signs are varying degree of HEARING LOSS; VERTIGO; and TINNITUS.
Diseases of the ninth cranial (glossopharyngeal) nerve or its nuclei in the medulla. The nerve may be injured by diseases affecting the lower brain stem, floor of the posterior fossa, jugular foramen, or the nerve's extracranial course. Clinical manifestations include loss of sensation from the pharynx, decreased salivation, and syncope. Glossopharyngeal neuralgia refers to a condition that features recurrent unilateral sharp pain in the tongue, angle of the jaw, external auditory meatus and throat that may be associated with SYNCOPE. Episodes may be triggered by cough, sneeze, swallowing, or pressure on the tragus of the ear. (Adams et al., Principles of Neurology, 6th ed, p1390)
An irregularly shaped venous space in the dura mater at either side of the sphenoid bone.
Filarial infection of the eyes transmitted from person to person by bites of Onchocerca volvulus-infected black flies. The microfilariae of Onchocerca are thus deposited beneath the skin. They migrate through various tissues including the eye. Those persons infected have impaired vision and up to 20% are blind. The incidence of eye lesions has been reported to be as high as 30% in Central America and parts of Africa.
Diseases of the trigeminal nerve or its nuclei, which are located in the pons and medulla. The nerve is composed of three divisions: ophthalmic, maxillary, and mandibular, which provide sensory innervation to structures of the face, sinuses, and portions of the cranial vault. The mandibular nerve also innervates muscles of mastication. Clinical features include loss of facial and intra-oral sensation and weakness of jaw closure. Common conditions affecting the nerve include brain stem ischemia, INFRATENTORIAL NEOPLASMS, and TRIGEMINAL NEURALGIA.
Diseases of the eleventh cranial (spinal accessory) nerve. This nerve originates from motor neurons in the lower medulla (accessory portion of nerve) and upper spinal cord (spinal portion of nerve). The two components of the nerve join and exit the skull via the jugular foramen, innervating the sternocleidomastoid and trapezius muscles, which become weak or paralyzed if the nerve is injured. The nerve is commonly involved in MOTOR NEURON DISEASE, and may be injured by trauma to the posterior triangle of the neck.
Diseases of the facial nerve or nuclei. Pontine disorders may affect the facial nuclei or nerve fascicle. The nerve may be involved intracranially, along its course through the petrous portion of the temporal bone, or along its extracranial course. Clinical manifestations include facial muscle weakness, loss of taste from the anterior tongue, hyperacusis, and decreased lacrimation.
Diseases of the sixth cranial (abducens) nerve or its nucleus in the pons. The nerve may be injured along its course in the pons, intracranially as it travels along the base of the brain, in the cavernous sinus, or at the level of superior orbital fissure or orbit. Dysfunction of the nerve causes lateral rectus muscle weakness, resulting in horizontal diplopia that is maximal when the affected eye is abducted and ESOTROPIA. Common conditions associated with nerve injury include INTRACRANIAL HYPERTENSION; CRANIOCEREBRAL TRAUMA; ISCHEMIA; and INFRATENTORIAL NEOPLASMS.
The 3d cranial nerve. The oculomotor nerve sends motor fibers to the levator muscles of the eyelid and to the superior rectus, inferior rectus, and inferior oblique muscles of the eye. It also sends parasympathetic efferents (via the ciliary ganglion) to the muscles controlling pupillary constriction and accommodation. The motor fibers originate in the oculomotor nuclei of the midbrain.
The articulation between the articular surface of the PATELLA and the patellar surface of the FEMUR.
Non-invasive methods of visualizing the CENTRAL NERVOUS SYSTEM, especially the brain, by various imaging modalities.
Diseases of the oculomotor nerve or nucleus that result in weakness or paralysis of the superior rectus, inferior rectus, medial rectus, inferior oblique, or levator palpebrae muscles, or impaired parasympathetic innervation to the pupil. With a complete oculomotor palsy, the eyelid will be paralyzed, the eye will be in an abducted and inferior position, and the pupil will be markedly dilated. Commonly associated conditions include neoplasms, CRANIOCEREBRAL TRAUMA, ischemia (especially in association with DIABETES MELLITUS), and aneurysmal compression. (From Adams et al., Principles of Neurology, 6th ed, p270)
Inflammation of the optic nerve. Commonly associated conditions include autoimmune disorders such as MULTIPLE SCLEROSIS, infections, and granulomatous diseases. Clinical features include retro-orbital pain that is aggravated by eye movement, loss of color vision, and contrast sensitivity that may progress to severe visual loss, an afferent pupillary defect (Marcus-Gunn pupil), and in some instances optic disc hyperemia and swelling. Inflammation may occur in the portion of the nerve within the globe (neuropapillitis or anterior optic neuritis) or the portion behind the globe (retrobulbar neuritis or posterior optic neuritis).
The middle of the three primitive cerebral vesicles of the embryonic brain. Without further subdivision, midbrain develops into a short, constricted portion connecting the PONS and the DIENCEPHALON. Midbrain contains two major parts, the dorsal TECTUM MESENCEPHALI and the ventral TEGMENTUM MESENCEPHALI, housing components of auditory, visual, and other sensorimoter systems.
Displacement of the PATELLA from the femoral groove.
A nerve which originates in the lumbar and sacral spinal cord (L4 to S3) and supplies motor and sensory innervation to the lower extremity. The sciatic nerve, which is the main continuation of the sacral plexus, is the largest nerve in the body. It has two major branches, the TIBIAL NERVE and the PERONEAL NERVE.
The flat, triangular bone situated at the anterior part of the KNEE.

Traumatic trochlear nerve palsy following minor occipital impact--four case reports. (1/41)

Four patients presented with transient trochlear nerve palsy following occipital impact. The impact was slight in all patients, and neuroimaging found no lesions of the nerve. Three patients had delayed onset. Two patients did not complain of diplopia, but were only aware of blurred vision. In such patients, the head tilting test was useful for diagnosis. Minor occipital impact can cause trochlear nerve palsy, which requires careful neurological examinations to identify.  (+info)

Infundibulohypophysitis in a man presenting with diabetes insipidus and cavernous sinus involvement. (2/41)

Infundibulohypophysitis is an unusual inflammatory condition that affects the infundibulum, the pituitary stalk, and the neurohypophysis and may be part of a range that includes lymphocytic hypophysitis. Lymphocytic hypophysitis occurs mainly in women and most often presents in the later stages of pregnancy. Infundibulohypophysitis usually presents with diabetes insipidus and the cause remains unclear. The case of a 46 year old man with a 12 week history of polyuria and polydipsia is reported. Cranial diabetes insipidus was diagnosed on the basis of a water deprivation test. Initial cranial and pituitary imaging studies were normal. He subsequently developed symptoms of panhypopituitism over a period of 6-9 months and then, more acutely, developed diplopia secondary to a fourth nerve palsy. Further brain imaging studies disclosed an enhancing pituitary stalk and a left cavernous sinus lesion. An initial trial of immunosuppressive treatment did not help symptoms significantly. The diagnosis of infundibulohypophysitis was made on histological evidence. The patient was treated with prednisolone and methotrexate. At 9 months he is well, without symptoms, and the radiological abnormalities have resolved.  (+info)

Presigmoid transpetrosal approach for the treatment of a large trochlear nerve schwannoma--case report. (3/41)

A 61-year-old man presented with a rare, large trochlear nerve schwannoma manifesting as left-sided weakness and hypesthesia, bilateral bulbar pareses, and trochlear nerve paresis persisting for 3 months. T1-weighted magnetic resonance imaging with gadolinium revealed an intensely enhanced, well-circumscribed lesion with multicystic formation occupying the prepontine and interpeduncular cisterns and compressing the pons and midbrain with greater extension to the right. The mass was completely removed through the presigmoid transpetrosal approach with preservation of the posterior cerebral, superior cerebellar, and basilar arteries and their branches. Neuroradiological examination after 3 years demonstrated no recurrence. Enlargement of a tumor in the cisternal portion is inclined to involve and/or encase the adjacent major arteries and their branches. The presigmoid transpetrosal approach is one of the best surgical routes to remove a large trochlear nerve schwannoma safely and completely.  (+info)

Adaptive neural mechanism for listing's law revealed in patients with fourth nerve palsy. (4/41)

PURPOSE: During fixation and saccades, human eye movements obey Listing's law, which specifies the eye's torsional angle as a function of its horizontal and vertical position. Torsion of the eye is in part controlled by the fourth nerve. This study investigates whether the brain adapts to defective torsional control after fourth nerve palsy. METHODS: Thirteen patients with fourth nerve palsy (11 chronic, 2 acute), and 10 normal subjects were studied with scleral search coils. With the head immobile, subjects made saccades to a target that moved between straight ahead and eight eccentric positions. At each target position, fixation was maintained for 3 seconds before the next saccade. From the eye position data, we computed the plane of best fit, referred to as Listing's plane. Violations of Listing's law were quantified by computing the "thickness" of this plane, defined as the SD of the distances to the plane from the data points. RESULTS: Both the paretic and nonparetic eyes in patients with chronic fourth nerve palsy obeyed Listing's law during fixation and saccades. However, Listing's planes in both eyes had abnormal orientations, being rotated temporally, meaning the eye excyclotorted during downgaze and incyclotorted during upgaze. In contrast, the paretic eye of patients with acute fourth nerve palsy violated Listing's law during saccades. During downward saccades, transient torsional deviations moved the paretic eye out of Listing's plane. Torsional drifts returned the paretic eye to Listing's plane during subsequent fixation. CONCLUSIONS: During saccades, acute fourth nerve palsy violates Listing's law, whereas chronic palsy obeys it, indicating that neural adaptation can restore Listing's law by adjusting the innervations to the remaining extraocular muscles, even when one eye muscle remains paretic. The transient torsional deviations during downward saccades in acute palsy are attributed to pulse-step mismatch, as a result of lesions in the trochlear nerve that lead to an imbalance of phasic and tonic signals reaching the muscles.  (+info)

The vestibulo-ocular reflex in fourth nerve palsy: deficits and adaptation. (5/41)

The effects of fourth nerve palsy on the vestibulo-ocular reflex (VOR) had not been systematically investigated. We used the magnetic scleral search coil technique to study the VOR in patients with unilateral fourth nerve palsy during sinusoidal head rotations in yaw, pitch and roll at different frequencies. In darkness, VOR gains are reduced during incyclotorsion, depression and abduction of the paretic eye, as anticipated from paresis of the superior oblique muscle. VOR gains during excyclotorsion, elevation and adduction of the paretic eye are also reduced, whereas gains in the non-paretic eye remain normal, indicating a selective adjustment of innervation to the paretic eye. In light, torsional visually enhanced VOR (VVOR) gains in the paretic eye remain reduced; however, visual input increases vertical and horizontal VVOR gains to normal in the paretic eye, without a conjugate increase in VVOR gains in the non-paretic eye, providing further evidence of selective adaptation in the paretic eye. Motions of the eyes after fourth nerve palsy exemplify monocular adaptation of the VOR, in response to peripheral neuromuscular deficits.  (+info)

Primary position and listing's law in acquired and congenital trochlear nerve palsy. (6/41)

PURPOSE: In ocular kinematics, the primary position (PP) of the eye is defined by the position from which movements do not induce ocular rotations around the line of sight (Helmholtz). PP is mathematically linked to the orientation of Listing's plane. This study was conducted to determine whether PP is affected differently in patients with clinically diagnosed congenital (conTNP) and acquired (acqTNP) trochlear nerve palsy. METHODS: Patients with unilateral conTNP (n = 25) and acqTNP (n = 9) performed a modified Hess screen test. Three-dimensional eye positions were recorded with dual search coils. RESULTS: PP in eyes with acqTNP was significantly more temporal (mean: 21.2 degrees ) than in eyes with conTNP (6.8 degrees ) or healthy eyes (7.2 degrees ). In the pooled data of all patients, the horizontal location of PP significantly correlated with vertical noncomitance with the paretic eye in adduction (R = 0.59). Using a computer model, PP in acqTNP could be reproduced by a neural lesion of the superior oblique (SO) muscle. An additional simulated overaction of the inferior oblique (IO) muscle moved PP back to normal, as in conTNP. Lengthening the SO and shortening the IO muscles could also simulate PP in conTNP. CONCLUSIONS: The temporal displacement of PP in acqTNP is a direct consequence of the reduced force of the SO muscle. The reversal of this temporal displacement of PP, which occurs in some patients with conTNP, can be explained by a secondary overaction of the IO muscle. Alternatively, length changes in the SO and IO muscles, or other anatomic anomalies within the orbit, without a neural lesion, may also explain the difference in location of PP between conTNP and acqTNP.  (+info)

Ocular rotation axes during dynamic Bielschowsky head-tilt testing in unilateral trochlear nerve palsy. (7/41)

PURPOSE: To explain the positive Bielschowsky head-tilt (BHT) sign in unilateral trochlear nerve palsy (uTNP) by the kinematics of three-dimensional eye rotations. METHODS: Twelve patients with uTNP monocularly fixed on targets on a Hess screen were oscillated (+/- 35 degrees, 0.3 Hz) about the roll axis on a motorized turntable (dynamic BHT). Three-dimensional eye movements were recorded with dual search coils. Normal data were collected from 11 healthy subjects. RESULTS: The rotation axis of the viewing paretic or unaffected eye was nearly parallel to the line of sight. The rotation axis of the covered fellow eye, however, was tilted inward relative to the other axis. This convergence of axes increased with gaze toward the unaffected side. Over entire cycles of head roll, the rotation axis of either eye remained relatively stable in both the viewing and covered conditions. CONCLUSIONS: In patients with uTNP, circular gaze trajectories of the covered paretic or unaffected eye during dynamic BHT are a direct consequence of the nasal deviation of the rotation axis from the line of sight. This, in turn, is a geometrical result of decreased force by the superior oblique muscle (SO) of the covered paretic eye or, according to Hering's law, increased force parallel to the paretic SO in the covered unaffected eye. The horizontal incomitance of rotation axes along horizontal eye positions can be explained by the same mechanism.  (+info)

Transient isolated trochlear nerve palsy associated with Rathke's cleft cyst. (8/41)

We report the case of a 52-year-old woman who developed vertical diplopia of 1-days duration. Neuro-ophthalmological testing revealed left trochlear nerve palsy, and sellar MRI revealed a 1.5 cm-sized pituitary mass lesion, a Rathke's cleft cyst. The diplopia disappeared spontaneously after 6 days.  (+info)

The trochlear nerve, also known as the fourth cranial nerve (CN IV), is a nerve that originates in the midbrain and innervates the superior oblique muscle of the eye. This muscle helps with the downward and outward movement of the eye, playing a crucial role in controlling eye movements and maintaining binocular vision. The trochlear nerve's main function is to provide motor (efferent) innervation to the superior oblique muscle, enabling fine-tuning of eye movements during activities such as reading, writing, or driving. Damage to this nerve can result in vertical diplopia (double vision), strabismus (eye misalignment), and other visual impairments.

The trochlear nerve, also known as the fourth cranial nerve (CN IV), is responsible for controlling the movement of the eye. It innervates the superior oblique muscle, which helps in depressing and rotating the eye downwards and outwards. Trochlear nerve diseases refer to conditions that affect this nerve and impair its function, leading to symptoms such as double vision (diplopia), vertical misalignment of the eyes, and difficulty with depth perception.

Trochlear nerve diseases can be caused by various factors, including trauma, compression, inflammation, infection, or tumors. Some common conditions that affect the trochlear nerve include:

1. Trochlear nerve palsy: This is a weakness or paralysis of the trochlear nerve, which can cause vertical and torsional diplopia, especially when looking downwards or to the side. It can be congenital or acquired due to trauma, compression, or other causes.
2. Aneurysm: Aneurysms in the vicinity of the trochlear nerve can compress or damage it, leading to palsy and diplopia.
3. Meningitis: Inflammation of the meninges (the membranes surrounding the brain and spinal cord) due to infection or other causes can affect the trochlear nerve and cause palsy.
4. Multiple sclerosis (MS): This is a chronic autoimmune disease that affects the central nervous system, including the cranial nerves. MS can cause demyelination of the trochlear nerve, leading to palsy and diplopia.
5. Diabetes: People with diabetes are at risk of developing diabetic neuropathy, which can affect any peripheral nerve, including the trochlear nerve.
6. Tumors: Space-occupying lesions in the brain or skull base, such as meningiomas, schwannomas, or pituitary adenomas, can compress the trochlear nerve and cause palsy.

The diagnosis of trochlear nerve diseases involves a thorough neurological examination, including assessment of eye movements and alignment. Imaging studies such as MRI or CT scans may be ordered to identify any structural lesions causing compression or damage to the nerve. Treatment depends on the underlying cause and may involve surgical intervention, medication, or observation.

A Trochlear nerve injury, also known as Fourth cranial nerve palsy, refers to damage or dysfunction of the fourth cranial nerve (trochlear nerve). This nerve is responsible for controlling the movement of the eye's superior oblique muscle, which helps in downward and outward movement of the eye.

Trochlear nerve injuries can result in vertical diplopia (double vision), where images appear double when looking downwards or to the side. The diplopia may be worse when looking down and out, such as when walking down stairs or reading.

The injury can be caused by various factors including head trauma, increased intracranial pressure, tumors, aneurysms, or other neurological conditions. Treatment options depend on the severity and cause of the injury and may include eye patches, prism lenses, or surgical intervention in some cases.

Optic nerve diseases refer to a group of conditions that affect the optic nerve, which transmits visual information from the eye to the brain. These diseases can cause various symptoms such as vision loss, decreased visual acuity, changes in color vision, and visual field defects. Examples of optic nerve diseases include optic neuritis (inflammation of the optic nerve), glaucoma (damage to the optic nerve due to high eye pressure), optic nerve damage from trauma or injury, ischemic optic neuropathy (lack of blood flow to the optic nerve), and optic nerve tumors. Treatment for optic nerve diseases varies depending on the specific condition and may include medications, surgery, or lifestyle changes.

The abducens nerve, also known as the sixth cranial nerve (CN VI), is a motor nerve that controls the lateral rectus muscle of the eye. This muscle is responsible for moving the eye away from the midline (towards the temple) and enables the eyes to look towards the side while keeping them aligned. Any damage or dysfunction of the abducens nerve can result in strabismus, where the eyes are misaligned and point in different directions, specifically an adduction deficit, also known as abducens palsy or sixth nerve palsy.

Olfactory nerve diseases refer to conditions that affect the olfactory nerve, which is the first cranial nerve responsible for the sense of smell. These diseases can result in impaired or loss of smell (anosmia) and taste (ageusia), as well as distorted perception of smells (parosmia). The causes of olfactory nerve diseases can include trauma, infection, inflammation, neurological disorders, and exposure to certain chemicals. Some examples of specific olfactory nerve diseases include sinusitis, upper respiratory infections, head injuries, and neurodegenerative disorders such as Parkinson's disease and Alzheimer's disease. Treatment for these conditions depends on the underlying cause and may include medications, surgery, or lifestyle changes.

Vagus nerve diseases, also known as vagus nerve disorders, refer to conditions that affect the functioning of the vagus nerve. The vagus nerve is the tenth cranial nerve and extends from the brainstem to the abdomen, playing a crucial role in regulating various automatic functions of the body such as heart rate, digestion, respiratory rate, and sweating.

Diseases of the vagus nerve can result from various causes, including inflammation, infection, trauma, compression, or degeneration. Some common vagus nerve disorders include:

1. Vagus nerve dysfunction: This is a general term used to describe any abnormality in the functioning of the vagus nerve. Symptoms may vary depending on the specific functions affected but can include difficulty swallowing, hoarseness, voice changes, and abnormal heart rate or blood pressure.
2. Vagus nerve neuropathy: This is a condition that results from damage to the vagus nerve fibers. It can cause symptoms such as difficulty swallowing, voice changes, and abnormal digestive function.
3. Gastroparesis: This is a condition in which the stomach muscles fail to contract properly, leading to delayed gastric emptying. Vagus nerve dysfunction is a common cause of gastroparesis.
4. Orthostatic hypotension: This is a condition characterized by a drop in blood pressure when standing up from a sitting or lying down position. Vagus nerve dysfunction can contribute to this condition by causing an abnormal response in the heart rate and blood vessels.
5. Inflammatory disorders: Certain inflammatory conditions such as rheumatoid arthritis, lupus, and sarcoidosis can affect the vagus nerve and cause various symptoms.

Treatment for vagus nerve diseases depends on the underlying cause and may include medications, surgery, or lifestyle changes.

Cranial nerve diseases refer to conditions that affect the cranial nerves, which are a set of 12 pairs of nerves that originate from the brainstem and control various functions in the head and neck. These functions include vision, hearing, taste, smell, movement of the eyes and face, and sensation in the face.

Diseases of the cranial nerves can result from a variety of causes, including injury, infection, inflammation, tumors, or degenerative conditions. The specific symptoms that a person experiences will depend on which cranial nerve is affected and how severely it is damaged.

For example, damage to the optic nerve (cranial nerve II) can cause vision loss or visual disturbances, while damage to the facial nerve (cranial nerve VII) can result in weakness or paralysis of the face. Other common symptoms of cranial nerve diseases include pain, numbness, tingling, and hearing loss.

Treatment for cranial nerve diseases varies depending on the underlying cause and severity of the condition. In some cases, medication or surgery may be necessary to treat the underlying cause and relieve symptoms. Physical therapy or rehabilitation may also be recommended to help individuals regain function and improve their quality of life.

The ophthalmic nerve, also known as the first cranial nerve or CN I, is a sensory nerve that primarily transmits information about vision, including light intensity and color, and sensation in the eye and surrounding areas. It is responsible for the sensory innervation of the upper eyelid, conjunctiva, cornea, iris, ciliary body, and nasal cavity. The ophthalmic nerve has three major branches: the lacrimal nerve, frontal nerve, and nasociliary nerve. Damage to this nerve can result in various visual disturbances and loss of sensation in the affected areas.

Diplopia is a medical term that refers to the condition where a person sees two images of a single object. It is commonly known as double vision. This can occur due to various reasons, such as nerve damage or misalignment of the eyes. Diplopia can be temporary or chronic and can affect one or both eyes. If you're experiencing diplopia, it's essential to consult an eye care professional for proper evaluation and treatment.

Cranial sinuses are a part of the venous system in the human head. They are air-filled spaces located within the skull and are named according to their location. The cranial sinuses include:

1. Superior sagittal sinus: It runs along the top of the brain, inside the skull, and drains blood from the scalp and the veins of the brain.
2. Inferior sagittal sinus: It runs along the bottom of the brain and drains into the straight sinus.
3. Straight sinus: It is located at the back of the brain and receives blood from the inferior sagittal sinus and great cerebral vein.
4. Occipital sinuses: They are located at the back of the head and drain blood from the scalp and skull.
5. Cavernous sinuses: They are located on each side of the brain, near the temple, and receive blood from the eye and surrounding areas.
6. Sphenoparietal sinus: It is a small sinus that drains blood from the front part of the brain into the cavernous sinus.
7. Petrosquamosal sinuses: They are located near the ear and drain blood from the scalp and skull.

The cranial sinuses play an essential role in draining blood from the brain and protecting it from injury.

Tolosa-Hunt syndrome is a rare disorder characterized by the inflammation of the nerve structures (including the fifth and sixth cranial nerves) within the cavernous sinus, a venous space near the base of the skull. This inflammation can lead to various symptoms such as:

1. Unilateral or bilateral orbital pain, which may be severe and deep, often radiating around the eye and temple.
2. Ophthalmoplegia (paralysis of the eye muscles), causing double vision (diplopia) and limited eye movement in specific directions.
3. Ptosis (drooping of the eyelid).
4. Other possible symptoms include decreased sensation around the forehead, cheek, or upper jaw, and loss of taste on the anterior part of the tongue.

The exact cause of Tolosa-Hunt syndrome is unknown, but it's believed to be related to an autoimmune response or a non-specific inflammatory process. It can also occur in conjunction with other medical conditions like neoplasms (tumors) or infections. The diagnosis typically involves imaging studies such as MRI and CT scans, along with blood tests and a thorough neurological examination.

Treatment usually includes corticosteroids to reduce inflammation and alleviate symptoms. In some cases, immunosuppressive medications or radiation therapy may be necessary. If left untreated, Tolosa-Hunt syndrome can lead to permanent visual impairment or other neurological deficits.

The term "cisterna magna" is derived from Latin, where "cisterna" means "reservoir" or "receptacle," and "magna" means "large." In medical anatomy, the cisterna magna refers to a large, sac-like space located near the lower part of the brainstem. It is a subarachnoid cistern, which means it is a space that contains cerebrospinal fluid (CSF) between the arachnoid and pia mater membranes covering the brain and spinal cord.

More specifically, the cisterna magna is situated between the cerebellum (the lower part of the brain responsible for coordinating muscle movements and maintaining balance) and the occipital bone (the bone at the back of the skull). This space contains a significant amount of CSF, which serves as a protective cushion for the brain and spinal cord, helps regulate intracranial pressure, and facilitates the circulation of nutrients and waste products.

The cisterna magna is an essential structure in neurosurgical procedures and diagnostic imaging techniques like lumbar puncture (spinal tap) or myelograms, where contrast agents are introduced into the CSF to visualize the spinal cord and surrounding structures. Additionally, it serves as a crucial landmark for various surgical approaches to the posterior fossa (the lower part of the skull that houses the cerebellum and brainstem).

Ophthalmoplegia is a medical term that refers to the paralysis or weakness of the eye muscles, which can result in double vision (diplopia) or difficulty moving the eyes. It can be caused by various conditions, including nerve damage, muscle disorders, or neurological diseases such as myasthenia gravis or multiple sclerosis. Ophthalmoplegia can affect one or more eye muscles and can be partial or complete. Depending on the underlying cause, ophthalmoplegia may be treatable with medications, surgery, or other interventions.

The hypoglossal nerve, also known as the 12th cranial nerve (CN XII), is primarily responsible for controlling tongue movements. Hypoglossal nerve diseases refer to conditions that affect this nerve and result in various tongue-related symptoms. These disorders can be congenital or acquired, and they may stem from different causes such as trauma, tumors, infections, inflammation, or degenerative processes.

Hypoglossal nerve diseases can present with the following symptoms:

1. Weakness or paralysis of the tongue muscles on one or both sides.
2. Deviation of the tongue towards the affected side when protruded.
3. Fasciculations (involuntary muscle twitches) or atrophy (wasting) of the tongue muscles.
4. Difficulty with speaking, swallowing, and chewing due to tongue weakness.
5. Changes in taste and sensation on the back of the tongue and throat.

Some specific hypoglossal nerve diseases include:

1. Hypoglossal nerve palsy: A condition characterized by unilateral or bilateral weakness or paralysis of the tongue due to damage to the hypoglossal nerve. Causes can include trauma, tumors, stroke, multiple sclerosis, or other neurological disorders.
2. Hypoglossal neuritis: Inflammation of the hypoglossal nerve, often caused by viral infections or autoimmune processes, leading to tongue weakness and atrophy.
3. Congenital hypoglossal nerve anomalies: Abnormal development of the hypoglossal nerve during fetal growth can result in various tongue-related symptoms and difficulties with speech and swallowing.
4. Tumors affecting the hypoglossal nerve: Both benign and malignant tumors, such as schwannomas or neurofibromas, can compress or infiltrate the hypoglossal nerve, causing weakness or paralysis.
5. Hypoglossal-facial anastomosis: A surgical procedure that connects the hypoglossal nerve to the facial nerve to restore facial movement in cases of facial nerve palsy. This connection can lead to tongue weakness as a side effect.

The oculomotor muscles are a group of extraocular muscles that control the movements of the eye. They include:

1. Superior rectus: This muscle is responsible for elevating the eye and helping with inward rotation (intorsion) when looking downwards.
2. Inferior rectus: It depresses the eye and helps with outward rotation (extorsion) when looking upwards.
3. Medial rectus: This muscle adducts, or moves, the eye towards the midline of the face.
4. Inferior oblique: The inferior oblique muscle intorts and elevates the eye.
5. Superior oblique: It extorts and depresses the eye.

These muscles work together to allow for smooth and precise movements of the eyes, enabling tasks such as tracking moving objects, reading, and maintaining visual fixation on a single point in space.

The vestibulocochlear nerve, also known as the 8th cranial nerve, is responsible for transmitting sound and balance information from the inner ear to the brain. Vestibulocochlear nerve diseases refer to conditions that affect this nerve and can result in hearing loss, vertigo, and balance problems.

These diseases can be caused by various factors, including genetics, infection, trauma, tumors, or degeneration. Some examples of vestibulocochlear nerve diseases include:

1. Vestibular neuritis: an inner ear infection that causes severe vertigo, nausea, and balance problems.
2. Labyrinthitis: an inner ear infection that affects both the vestibular and cochlear nerves, causing vertigo, hearing loss, and tinnitus.
3. Acoustic neuroma: a benign tumor that grows on the vestibulocochlear nerve, causing hearing loss, tinnitus, and balance problems.
4. Meniere's disease: a inner ear disorder that causes vertigo, hearing loss, tinnitus, and a feeling of fullness in the ear.
5. Ototoxicity: damage to the inner ear caused by certain medications or chemicals that can result in hearing loss and balance problems.
6. Vestibular migraine: a type of migraine that is associated with vertigo, dizziness, and balance problems.

Treatment for vestibulocochlear nerve diseases varies depending on the specific condition and its severity. It may include medication, physical therapy, surgery, or a combination of these approaches.

The glossopharyngeal nerve, also known as the ninth cranial nerve (CN IX), is primarily responsible for providing motor innervation to the stylopharyngeus muscle and sensory innervation to parts of the pharynx, middle ear, and posterior tongue. It also plays a role in the reflexive control of heart rate via the baroreceptors located in the carotid sinus.

Glossopharyngeal nerve diseases refer to conditions that affect the function of this nerve, leading to various symptoms. These diseases can be classified into two main categories: peripheral and central. Peripheral disorders are caused by damage or injury to the nerve itself, while central disorders result from problems in the brainstem where the glossopharyngeal nerve originates.

Some examples of glossopharyngeal nerve diseases include:

1. Glossopharyngeal neuralgia: A rare condition characterized by severe, stabbing pain in the throat, ear, or tongue, often triggered by swallowing or talking. This disorder may be caused by compression of the nerve by blood vessels or other structures.

2. Infections: Bacterial and viral infections can cause inflammation and damage to the glossopharyngeal nerve, leading to dysfunction. Examples include Lyme disease, herpes zoster (shingles), and meningitis.

3. Tumors: Benign or malignant growths in the head and neck region can compress and injure the glossopharyngeal nerve, resulting in symptoms related to its dysfunction.

4. Trauma: Direct trauma to the neck or skull base can damage the glossopharyngeal nerve, causing various deficits depending on the severity of the injury.

5. Neurological disorders: Conditions such as multiple sclerosis and stroke can affect the central connections of the glossopharyngeal nerve in the brainstem, leading to dysfunction.

6. Genetic conditions: Rare genetic disorders like Moersch-Woltman syndrome (also known as stiff person syndrome) can involve the glossopharyngeal nerve and cause symptoms related to its dysfunction.

Symptoms of glossopharyngeal nerve dysfunction may include difficulty swallowing, hoarseness, loss of taste on the back of the tongue, decreased sensation in the throat or ear, and pain in the neck, throat, or ear. Treatment for these conditions depends on the underlying cause and may involve medications, surgery, or other interventions to address the specific problem.

The cavernous sinus is a venous structure located in the middle cranial fossa, which is a depression in the skull that houses several important nerves and blood vessels. The cavernous sinus is situated on either side of the sphenoid bone, near the base of the skull, and it contains several important structures:

* The internal carotid artery, which supplies oxygenated blood to the brain
* The abducens nerve (cranial nerve VI), which controls lateral movement of the eye
* The oculomotor nerve (cranial nerve III), which controls most of the muscles that move the eye
* The trochlear nerve (cranial nerve IV), which controls one of the muscles that moves the eye
* The ophthalmic and maxillary divisions of the trigeminal nerve (cranial nerve V), which transmit sensory information from the face and head

The cavernous sinus is an important structure because it serves as a conduit for several critical nerves and blood vessels. However, it is also vulnerable to various pathological conditions such as thrombosis (blood clots), infection, tumors, or aneurysms, which can lead to serious neurological deficits or even death.

Onchocerciasis, Ocular is a medical condition that specifically refers to the eye manifestations caused by the parasitic infection, Onchocerca volvulus. Also known as "river blindness," this disease is spread through the bite of infected blackflies.

Ocular onchocerciasis affects various parts of the eye, including the conjunctiva, cornea, iris, and retina. The infection can cause symptoms such as itching, burning, and redness of the eyes. Over time, it may lead to more serious complications like punctate keratitis (small, scattered opacities on the cornea), cataracts, glaucoma, and ultimately, blindness.

The infection is diagnosed through a skin snip or blood test, which can detect the presence of microfilariae (the larval stage of the parasite) or antibodies against the parasite. Treatment typically involves administering oral medications such as ivermectin, which kills the microfilariae and reduces the risk of eye damage. However, it does not kill the adult worms, so multiple doses are often required to control the infection. In some cases, surgery may be necessary to remove advanced ocular lesions.

Trigeminal nerve diseases refer to conditions that affect the trigeminal nerve, which is one of the cranial nerves responsible for sensations in the face and motor functions such as biting and chewing. The trigeminal nerve has three branches: ophthalmic, maxillary, and mandibular, which innervate different parts of the face and head.

Trigeminal nerve diseases can cause various symptoms, including facial pain, numbness, tingling, or weakness. Some common trigeminal nerve diseases include:

1. Trigeminal neuralgia: A chronic pain condition that affects the trigeminal nerve, causing intense, stabbing, or electric shock-like pain in the face.
2. Hemifacial spasm: A neuromuscular disorder that causes involuntary muscle spasms on one side of the face, often affecting the muscles around the eye and mouth.
3. Trigeminal neuropathy: Damage or injury to the trigeminal nerve, which can result in numbness, tingling, or weakness in the face.
4. Herpes zoster oticus (Ramsay Hunt syndrome): A viral infection that affects the facial nerve and geniculate ganglion of the trigeminal nerve, causing facial paralysis, ear pain, and a rash around the ear.
5. Microvascular compression: Compression of the trigeminal nerve by a blood vessel, which can cause symptoms similar to trigeminal neuralgia.

Treatment for trigeminal nerve diseases depends on the specific condition and its severity. Treatment options may include medication, surgery, or radiation therapy.

The accessory nerve, also known as the 11th cranial nerve (CN XI), has both a cranial and spinal root and innervates the sternocleidomastoid muscle and trapezius muscle. Accessory nerve diseases refer to conditions that affect the function of this nerve, leading to weakness or paralysis of the affected muscles.

Some examples of accessory nerve diseases include:

1. Traumatic injury: Direct trauma to the neck or posterior scalene region can damage the spinal root of the accessory nerve. This can result in weakness or paralysis of the trapezius muscle, leading to difficulty with shoulder movement and pain.
2. Neuralgia: Accessory nerve neuralgia is a condition characterized by painful spasms or shooting pains along the course of the accessory nerve. It can be caused by nerve compression, inflammation, or injury.
3. Tumors: Tumors in the neck region, such as schwannomas or neurofibromas, can compress or invade the accessory nerve, leading to weakness or paralysis of the affected muscles.
4. Infections: Viral infections, such as poliovirus or West Nile virus, can cause inflammation and damage to the accessory nerve, resulting in weakness or paralysis.
5. Neuropathy: Accessory nerve neuropathy is a condition characterized by degeneration of the accessory nerve fibers due to various causes such as diabetes, autoimmune disorders, or exposure to toxins. This can result in weakness or paralysis of the affected muscles.
6. Congenital defects: Some individuals may be born with congenital defects that affect the development and function of the accessory nerve, leading to weakness or paralysis of the affected muscles.

Treatment for accessory nerve diseases depends on the underlying cause and can include physical therapy, medications, surgery, or a combination of these approaches.

Facial nerve diseases refer to a group of medical conditions that affect the function of the facial nerve, also known as the seventh cranial nerve. This nerve is responsible for controlling the muscles of facial expression, and it also carries sensory information from the taste buds in the front two-thirds of the tongue, and regulates saliva flow and tear production.

Facial nerve diseases can cause a variety of symptoms, depending on the specific location and extent of the nerve damage. Common symptoms include:

* Facial weakness or paralysis on one or both sides of the face
* Drooping of the eyelid and corner of the mouth
* Difficulty closing the eye or keeping it closed
* Changes in taste sensation or dryness of the mouth and eyes
* Abnormal sensitivity to sound (hyperacusis)
* Twitching or spasms of the facial muscles

Facial nerve diseases can be caused by a variety of factors, including:

* Infections such as Bell's palsy, Ramsay Hunt syndrome, and Lyme disease
* Trauma or injury to the face or skull
* Tumors that compress or invade the facial nerve
* Neurological conditions such as multiple sclerosis or Guillain-Barre syndrome
* Genetic disorders such as Moebius syndrome or hemifacial microsomia

Treatment for facial nerve diseases depends on the underlying cause and severity of the symptoms. In some cases, medication, physical therapy, or surgery may be necessary to restore function and relieve symptoms.

The abducens nerve, also known as the sixth cranial nerve, is responsible for controlling the lateral rectus muscle of the eye, which enables the eye to move outward. Abducens nerve diseases refer to conditions that affect this nerve and can result in various symptoms, primarily affecting eye movement.

Here are some medical definitions related to abducens nerve diseases:

1. Abducens Nerve Palsy: A condition characterized by weakness or paralysis of the abducens nerve, causing difficulty in moving the affected eye outward. This results in double vision (diplopia), especially when gazing towards the side of the weakened nerve. Abducens nerve palsy can be congenital, acquired, or caused by various factors such as trauma, tumors, aneurysms, infections, or diseases like diabetes and multiple sclerosis.
2. Sixth Nerve Palsy: Another term for abducens nerve palsy, referring to the weakness or paralysis of the sixth cranial nerve.
3. Internuclear Ophthalmoplegia (INO): A neurological condition affecting eye movement, often caused by a lesion in the medial longitudinal fasciculus (MLF), a bundle of nerve fibers that connects the abducens nucleus with the oculomotor nucleus. INO results in impaired adduction (inward movement) of the eye on the side of the lesion and nystagmus (involuntary eye movements) of the abducting eye on the opposite side when attempting to look towards the side of the lesion.
4. One-and-a-Half Syndrome: A rare neurological condition characterized by a combination of INO and internuclear ophthalmoplegia with horizontal gaze palsy on the same side, caused by damage to both the abducens nerve and the paramedian pontine reticular formation (PPRF). This results in limited or no ability to move the eyes towards the side of the lesion and impaired adduction of the eye on the opposite side.
5. Brainstem Encephalitis: Inflammation of the brainstem, which can affect the abducens nerve and other cranial nerves, leading to various neurological symptoms such as diplopia (double vision), ataxia (loss of balance and coordination), and facial weakness. Brainstem encephalitis can be caused by infectious agents, autoimmune disorders, or paraneoplastic syndromes.
6. Multiple Sclerosis (MS): An autoimmune disorder characterized by inflammation and demyelination of the central nervous system, including the brainstem and optic nerves. MS can cause various neurological symptoms, such as diplopia, nystagmus, and INO, due to damage to the abducens nerve and other cranial nerves.
7. Wernicke's Encephalopathy: A neurological disorder caused by thiamine (vitamin B1) deficiency, often seen in alcoholics or individuals with malnutrition. Wernicke's encephalopathy can affect the brainstem and cause various symptoms such as diplopia, ataxia, confusion, and oculomotor abnormalities.
8. Pontine Glioma: A rare type of brain tumor that arises from the glial cells in the pons (a part of the brainstem). Pontine gliomas can cause various neurological symptoms such as diplopia, facial weakness, and difficulty swallowing due to their location in the brainstem.
9. Brainstem Cavernous Malformation: A benign vascular lesion that arises from the small blood vessels in the brainstem. Brainstem cavernous malformations can cause various neurological symptoms such as diplopia, ataxia, and facial weakness due to their location in the brainstem.
10. Pituitary Adenoma: A benign tumor that arises from the pituitary gland, located at the base of the brain. Large pituitary adenomas can compress the optic nerves and cause various visual symptoms such as diplopia, visual field defects, and decreased vision.
11. Craniopharyngioma: A benign tumor that arises from the remnants of the Rathke's pouch, a structure that gives rise to the anterior pituitary gland. Craniopharyngiomas can cause various neurological and endocrine symptoms such as diplopia, visual field defects, headaches, and hormonal imbalances due to their location near the optic nerves and pituitary gland.
12. Meningioma: A benign tumor that arises from the meninges, the protective covering of the brain and spinal cord. Meningiomas can cause various neurological symptoms such as diplopia, headaches, and seizures depending on their location in the brain or spinal cord.
13. Chordoma: A rare type of malignant tumor that arises from the remnants of the notochord, a structure that gives rise to the spine during embryonic development. Chordomas can cause various neurological and endocrine symptoms such as diplopia, visual field defects, headaches, and hormonal imbalances due to their location near the brainstem and spinal cord.
14. Metastatic Brain Tumors: Malignant tumors that spread from other parts of the body to the brain. Metastatic brain tumors can cause various neurological symptoms such as diplopia, headaches, seizures, and cognitive impairment depending on their location in the brain.
15. Other Rare Brain Tumors: There are many other rare types of brain tumors that can cause diplopia or other neurological symptoms, including gliomas, ependymomas, pineal region tumors, and others. These tumors require specialized diagnosis and treatment by neuro-oncologists and neurosurgeons with expertise in these rare conditions.

In summary, diplopia can be caused by various brain tumors, including pituitary adenomas, meningiomas, chordomas, metastatic brain tumors, and other rare types of tumors. It is important to seek medical attention promptly if you experience diplopia or other neurological symptoms, as early diagnosis and treatment can improve outcomes and quality of life.

The oculomotor nerve, also known as the third cranial nerve (CN III), is a motor nerve that originates from the midbrain. It controls the majority of the eye muscles, including the levator palpebrae superioris muscle that raises the upper eyelid, and the extraocular muscles that enable various movements of the eye such as looking upward, downward, inward, and outward. Additionally, it carries parasympathetic fibers responsible for pupillary constriction and accommodation (focusing on near objects). Damage to this nerve can result in various ocular motor disorders, including strabismus, ptosis, and pupillary abnormalities.

The patellofemoral joint is the articulation between the patella (kneecap) and the femur (thigh bone). It is a synovial joint, which means it is surrounded by a joint capsule containing synovial fluid to lubricate the joint. This joint is responsible for providing stability to the knee extensor mechanism and allows for smooth movement of the patella during activities like walking, running, and jumping. Pain or dysfunction in this joint can result in various conditions such as patellofemoral pain syndrome, chondromalacia patella, or patellar dislocation.

Neuroimaging is a medical term that refers to the use of various techniques to either directly or indirectly image the structure, function, or pharmacology of the nervous system. It includes techniques such as computed tomography (CT), magnetic resonance imaging (MRI), functional MRI (fMRI), positron emission tomography (PET), single-photon emission computed tomography (SPECT), and diffusion tensor imaging (DTI). These techniques are used to diagnose and monitor various neurological and psychiatric conditions, as well as to understand the underlying mechanisms of brain function in health and disease.

The oculomotor nerve, also known as the third cranial nerve (CN III), is responsible for controlling several important eye movements and functions. Oculomotor nerve diseases refer to conditions that affect this nerve and can lead to various symptoms related to eye movement and function. Here's a medical definition of oculomotor nerve diseases:

Oculomotor nerve diseases are a group of medical disorders characterized by the dysfunction or damage to the oculomotor nerve (CN III), resulting in impaired eye movements, abnormalities in pupillary response, and potential effects on eyelid position. These conditions can be congenital, acquired, or traumatic in nature and may lead to partial or complete paralysis of the nerve. Common oculomotor nerve diseases include oculomotor nerve palsy, third nerve ganglionopathies, and compressive oculomotor neuropathies caused by various pathologies such as aneurysms, tumors, or infections.

Optic neuritis is a medical condition characterized by inflammation and damage to the optic nerve, which transmits visual information from the eye to the brain. This condition can result in various symptoms such as vision loss, pain with eye movement, color vision disturbances, and pupillary abnormalities. Optic neuritis may occur in isolation or be associated with other underlying medical conditions, including multiple sclerosis, neuromyelitis optica, and autoimmune disorders. The diagnosis typically involves a comprehensive eye examination, including visual acuity testing, dilated funduscopic examination, and possibly imaging studies like MRI to evaluate the optic nerve and brain. Treatment options may include corticosteroids or other immunomodulatory therapies to reduce inflammation and prevent further damage to the optic nerve.

The mesencephalon, also known as the midbrain, is the middle portion of the brainstem that connects the hindbrain (rhombencephalon) and the forebrain (prosencephalon). It plays a crucial role in several important functions including motor control, vision, hearing, and the regulation of consciousness and sleep-wake cycles. The mesencephalon contains several important structures such as the cerebral aqueduct, tectum, tegmentum, cerebral peduncles, and several cranial nerve nuclei (III and IV).

Patellar dislocation is a medical condition characterized by the displacement of the patella (kneecap) from its normal position in the femoral groove, which is a part of the femur (thighbone). This displacement usually occurs laterally, meaning that the patella moves toward the outer side of the knee.

Patellar dislocation can happen as a result of direct trauma or due to various factors that increase the laxity of the medial patellofemoral ligament and tightness of the lateral structures, leading to abnormal tracking of the patella. These factors include anatomical variations, muscle imbalances, genetic predisposition, or degenerative changes in the knee joint.

Dislocation of the patella can cause pain, swelling, and difficulty in moving the knee. In some cases, it might be associated with other injuries such as fractures or damage to the articular cartilage and surrounding soft tissues. Immediate medical attention is required for proper diagnosis and treatment, which may involve reduction, immobilization, physical therapy, bracing, or even surgery in severe cases.

The sciatic nerve is the largest and longest nerve in the human body, running from the lower back through the buttocks and down the legs to the feet. It is formed by the union of the ventral rami (branches) of the L4 to S3 spinal nerves. The sciatic nerve provides motor and sensory innervation to various muscles and skin areas in the lower limbs, including the hamstrings, calf muscles, and the sole of the foot. Sciatic nerve disorders or injuries can result in symptoms such as pain, numbness, tingling, or weakness in the lower back, hips, legs, and feet, known as sciatica.

The patella, also known as the kneecap, is a sesamoid bone located at the front of the knee joint. It is embedded in the tendon of the quadriceps muscle and serves to protect the knee joint and increase the leverage of the extensor mechanism, allowing for greater extension force of the lower leg. The patella moves within a groove on the femur called the trochlea during flexion and extension of the knee.

Information on Familial congenital palsy of trochlear nerve, which may include symptoms, causes, inheritance, treatments, ... Familial congenital palsy of trochlear nerve is a rare, genetic, neuro- ophthalmological disease characterized by congenital ... Dont fight Familial congenital palsy of trochlear nerve alone.. Find your community on the free RareGuru App. Connect with ... Connect with other users with Familial congenital palsy of trochlear nerve on the RareGuru app Get the Free App!. ...
Trochlear nerve palsy is mentioned in ophthalmology texts dating to the mid nineteenth century. However, it received little ... there were only 657 cases of isolated fourth nerve disease. [6] Fourth nerve palsy also was the least frequent in a pediatric ... encoded search term (Trochlear Nerve Palsy (Fourth Nerve Palsy)) and Trochlear Nerve Palsy (Fourth Nerve Palsy) What to Read ... Acquired Trochlear Nerve Palsy. The long course of the trochlear nerve makes it especially susceptible to injury in association ...
... congenital cataract Bilateral optic nerve hypoplasia Idiopathic Lebers congenital amaurosis Optic nerve or macular disease ... sclerosis Stroke Thalamic hemorrhage Trauma Tumor Infantile cerebellar retinal degeneration Non-physiological Trochlear nerve ... syndrome Ménières disease and other balance disorders Multiple sclerosis Optic nerve hypoplasia Pelizaeus-Merzbacher disease ... Some of the diseases that present nystagmus as a pathological sign or symptom are as follows: Aniridia Benign paroxysmal ...
Dive into the research topics of Trochlear nerve schwannoma with intratumoral hemorrhage: case report.. Together they form a ...
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TRIGEMINAL NERVE DISEASES ENFERMEDADES DEL NERVIO TRIGEMINO DOENÇAS DO NERVO TRIGÊMEO TROCHLEAR NERVE DISEASES ENFERMEDADES DEL ... ABDUCENS NERVE DISEASES ENFERMEDADES DEL NERVIO ABDUCENTE DOENÇAS DO NERVO ABDUCENTE ABDUCENS NERVE INJURY TRAUMATISMO DEL ... ACCESSORY NERVE DISEASES ENFERMEDADES DEL NERVIO ACCESORIO DOENÇAS DO NERVO ACESSÓRIO ACUPUNCTURE, EAR ACUPUNTURA EN EL OIDO ... OLFACTORY NERVE DISEASES ENFERMEDADES DEL NERVIO OLFATORIO DOENÇAS DO NERVO OLFATÓRIO OMEGA-AGATOXIN IVA OMEGA-AGATOXINA IVA ...
TRIGEMINAL NERVE DISEASES ENFERMEDADES DEL NERVIO TRIGEMINO DOENÇAS DO NERVO TRIGÊMEO TROCHLEAR NERVE DISEASES ENFERMEDADES DEL ... ABDUCENS NERVE DISEASES ENFERMEDADES DEL NERVIO ABDUCENTE DOENÇAS DO NERVO ABDUCENTE ABDUCENS NERVE INJURY TRAUMATISMO DEL ... ACCESSORY NERVE DISEASES ENFERMEDADES DEL NERVIO ACCESORIO DOENÇAS DO NERVO ACESSÓRIO ACUPUNCTURE, EAR ACUPUNTURA EN EL OIDO ... OLFACTORY NERVE DISEASES ENFERMEDADES DEL NERVIO OLFATORIO DOENÇAS DO NERVO OLFATÓRIO OMEGA-AGATOXIN IVA OMEGA-AGATOXINA IVA ...
TRIGEMINAL NERVE DISEASES ENFERMEDADES DEL NERVIO TRIGEMINO DOENÇAS DO NERVO TRIGÊMEO TROCHLEAR NERVE DISEASES ENFERMEDADES DEL ... ABDUCENS NERVE DISEASES ENFERMEDADES DEL NERVIO ABDUCENTE DOENÇAS DO NERVO ABDUCENTE ABDUCENS NERVE INJURY TRAUMATISMO DEL ... ACCESSORY NERVE DISEASES ENFERMEDADES DEL NERVIO ACCESORIO DOENÇAS DO NERVO ACESSÓRIO ACUPUNCTURE, EAR ACUPUNTURA EN EL OIDO ... OLFACTORY NERVE DISEASES ENFERMEDADES DEL NERVIO OLFATORIO DOENÇAS DO NERVO OLFATÓRIO OMEGA-AGATOXIN IVA OMEGA-AGATOXINA IVA ...
A knowledge graph of biological entities such as genes, gene functions, diseases, phenotypes and chemicals. Embeddings are ... trochlear nerve disease DOID:13864 * Paraplegia HP:0010550 * KIAA1217 http://www.ncbi.nlm.nih.gov/gene/56243 ...
Ranked list of possible diseases from either several symptoms or a full patient history. A similarity measure between symptoms ... Median Nerve Diseases. On-line free medical diagnosis assistant. ... Peripheral Nerve Injuries. 2. + + 22. Trochlear Nerve Diseases ... Diseases. Frequent searches. Medicinal plants. Health topics. Medical dictionary. Health sites. Questions and answers. ...
Trochlear Nerve Diseases 27% * Horner Syndrome 23% * Disorders of Excessive Somnolence 23% ... Is Alzheimer Disease an Autoimmune Disorder?. Bertholf, R. L., Jan 31 2021, (E-pub ahead of print) In: The journal of applied ... In vitro and pilot in vivo imaging of 18 kDa translocator protein (TSPO) in inflammatory vascular disease. Schollhammer, R., ... Lifes Simple 7 and Nonalcoholic Fatty Liver Disease: The Multiethnic Study of Atherosclerosis. Oni, E., Ogunmoroti, O., Allen ...
Trochlear nerve cavernous hemangioma (CH) is a rare disease. There have been only five such cases reported in the world ... with a diagnosis of trochlear nerve CH confirmed by pathological examination. Further nerve anastomosis was not adopted, and ... The authors report a case of trochlear nerve CH in the Asian population and review the relevant literature. A 49-year-old Asian ... Physical examination identified a complete paralysis of left trochlear nerve. In imaging, a circular lesion measuring about 1 ...
Familial congenital palsy of trochlear nerve From NCATS Genetic and Rare Diseases Information Center ... Selected Rare Diseases. Browse full list of rare diseases A-Z *Alpha-1 Antitrypsin Deficiency ... Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it ...
Nerve Palsy - Etiology, pathophysiology, symptoms, signs, diagnosis & prognosis from the MSD Manuals - Medical Professional ... Infarction due to small-vessel disease (eg, in diabetes). Rarely, this palsy results from aneurysms, tumors (eg, tentorial ... optic nerve, or extraocular muscles and their nerves; thus, they can be considered cranial nerve disorders, neuro- ... See also Overview of Neuro-ophthalmologic and Cranial Nerve Disorders Overview of Neuro-ophthalmologic and Cranial Nerve ...
21] Dense concentrations of GQ1b ganglioside are found in the oculomotor, trochlear, and abducens nerves, which may explain the ... GBS is considered to be a postinfectious, immune-mediated disease targeting peripheral nerves. Up to two thirds of patients ... Pathologic findings in GBS include lymphocytic infiltration of spinal roots and peripheral nerves (cranial nerves may be ... the only infectious disease laboratories capable of making this diagnosis are at the US Centers for Disease Control and ...
Trochlear nerve palsy. Uveitis and ocular inflammation. Visual disturbances. Visual field loss. Vitreoretinal diseases ... Ocular surface disease. Oculomotor nerve palsy. Open-angle glaucoma. Optic nerve atrophy. Optic nerve drusen. Optic nerve ... Graves disease/thyroid-associated ophthalmopathy. Hemifacial spasm. Herpes-related eye disease. Herpetic eye infection. Higher ... External disease. Eye movement disorders. Eye trauma. Eyelid "bags" and facial "wrinkles". Eyelid and facial spasm. Eyelid ...
Optic Nerve Diseases. Trigeminal Nerve Diseases. Trochlear Nerve Diseases. Vagus Nerve Diseases ...
Optic Nerve Diseases Medicine & Life Sciences 40% * Trochlear Nerve Medicine & Life Sciences 40% ...
Cranial nerve IV (trochlear nerve). They include the nerves that transmit smell, those responsible for vision and the movement ... complications 4 Cs Coronary Artery Disease Coronary Rheumatic Fever Congestive Heart Failure The symptoms can often be ... II Optic Nerve. Cranial nerves- OH OH OH TO TOUCH AND FEEL A GIRLS VAGINA AH HEAVEN. oh oh oh to touch and feel cranial nerves ... The third cranial nerve, also called the oculomotor nerve. olfactory optic oculomotor trochlear trigeminal Abducens f Context. ...
Diseases of the eye muscles or oculomotor cranial nerves (III, IV, and VI) are considered infranuclear. Nuclear disorders are ... caused by disease of the oculomotor, trochlear, or abducens nuclei in the BRAIN STEM. Supranuclear disorders are produced by ... CENTRAL NERVOUS SYSTEM DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; NEUROMUSCULAR DISEASES; or MUSCULAR DISEASES.. ... Tibial Nerve. The medial terminal branch of the sciatic nerve. The tibial nerve fibers originate in lumbar and sacral spinal ...
Optic Nerve Diseases [C10.292.700] * Trochlear Nerve Diseases [C10.292.850] * Vagus Nerve Diseases [C10.292.887] ... Nervous System Diseases [C10] * Cranial Nerve Diseases [C10.292] * Abducens Nerve Diseases [C10.292.150] ... Typically, ABDUCENS NERVE; OCULOMOTOR NERVE; and TROCHLEAR NERVE are involved with DIPLOPIA and BLEPHAROPTOSIS.. Terms. ... Typically, ABDUCENS NERVE; OCULOMOTOR NERVE; and TROCHLEAR NERVE are involved with DIPLOPIA and BLEPHAROPTOSIS.. Entry Term(s) ...
21] Dense concentrations of GQ1b ganglioside are found in the oculomotor, trochlear, and abducens nerves, which may explain the ... GBS is considered to be a postinfectious, immune-mediated disease targeting peripheral nerves. Up to two thirds of patients ... Pathologic findings in GBS include lymphocytic infiltration of spinal roots and peripheral nerves (cranial nerves may be ... Common complaints associated with cranial nerve involvement in GBS include the following:. * Facial droop (may mimic Bell palsy ...

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