A syndrome associated with defective sympathetic innervation to one side of the face, including the eye. Clinical features include MIOSIS; mild BLEPHAROPTOSIS; and hemifacial ANHIDROSIS (decreased sweating)(see HYPOHIDROSIS). Lesions of the BRAIN STEM; cervical SPINAL CORD; first thoracic nerve root; apex of the LUNG; CAROTID ARTERY; CAVERNOUS SINUS; and apex of the ORBIT may cause this condition. (From Miller et al., Clinical Neuro-Ophthalmology, 4th ed, pp500-11)
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.
Dilation of pupils to greater than 6 mm combined with failure of the pupils to constrict when stimulated with light. This condition may occur due to injury of the pupillary fibers in the oculomotor nerve, in acute angle-closure glaucoma, and in ADIE SYNDROME.
The splitting of the vessel wall in one or both (left and right) internal carotid arteries (CAROTID ARTERY, INTERNAL). Interstitial hemorrhage into the media of the vessel wall can lead to occlusion of the internal carotid artery and aneurysm formation.

Isolated Horner's syndrome and syringomyelia. (1/97)

Although syringomyelia has been associated with Horner's syndrome, it is typically associated with other neurological findings such as upper limb weakness or numbness. A patient is described who had an isolated Horner's syndrome as the only manifestation of syringomyelia. A 76 year old woman was discovered to have right upper lid ptosis and right pupillary miosis. Neurological examination was unremarkable, and pharmacological testing was consistent with localisation of the lesion to a first or second order sympathetic neuron. Neuroimaging disclosed a Chiari I malformation with a syrinx extending to the C2 to C4 level. An isolated Horner's syndrome may be the presenting manifestation of syringomyelia.  (+info)

Course and distribution of facial corticobulbar tract fibres in the lower brain stem. (2/97)

The course and distribution of the facial corticobulbar tract (CBT) was examined by correlating MRI of brain stem lesions with neurological symptoms and signs including central (C-FP) or peripheral facial paresis (P-FP) in 70 patients with localised infarction of the lower brain stem. C-FP occurred more often in patients with lesions of the lower pons or upper medulla of the ventromedial brain stem. Some patients with dorsolateral infarcts of the upper medulla to the lower pons showed C-FP, mostly on the lesion side. P-FP on the side of the lesion was also seen in patients with dorsolateral involvement of the lower pons. Patients with ventromedial infarction of the brain stem showed paresis of extremities contralateral to the lesion. Specific neurological symptoms and signs such as dysphagia, vertigo, nystagmus, Horner's syndrome, ipsilateral cerebellar ataxia, and contralateral superficial sensory impairment were seen in patients with dorsolateral infarcts of the brain stem. It is hypothesised that the facial CBT descends at the ventromedial lower pons, near the corticospinal tract, mainly to the level of the upper medulla, where the fibres then decussate and ascend in the dorsolateral medulla to synapse in the contralateral facial nucleus.  (+info)

First rib fracture: a hallmark of severe trauma. (3/97)

First rib fractures occurred in 55 patients. This injury is a harbinger of major trauma with 35 patients suffering a major chest injury, and abdominal and cardiac injuries occurring in 18 and eight patients respectively. The mortality associated with this injury was high (36.3%). Neurologic lesions accounted for the majority of deaths, however, unrecognized abdominal injuries and pulmonary complications were significant causes of mortality. Brachial plexus injury (5) and Horner's syndrome (3) occurred in survivors. Three patients had an associated injury of the subclavian artery, and the importance of this association is stressed. One late-developing post-traumatic thoracic outlet syndrome occurred. A fracture of the first rib is a hallmark of severe trauma; its presence should alert the clinician to: 1) generalized massive trauma with abdominal, chest, and cardiac injuries; 2) local injury to the subclavian artery and brachial plexus and; 3) necessity of long-term followup for late-developing sequelae.  (+info)

A case of Brown-Sequard syndrome with associated Horner's syndrome after blunt injury to the cervical spine. (4/97)

A 26 year old motorcyclist was received by the trauma team in our accident and emergency department after a head on collision with a motor vehicle. He had been correctly immobilised and his primary survey was essentially normal. He was alert and orientated with a Glasgow Coma score of 15 and had no symptoms or signs of spinal injury. His cervical spine radiography was also normal. Neurological examination however, revealed anisocoria, his left pupil being smaller than his right, and a Brown-Sequard syndrome, with a sensory level at C6. Immobilisation was maintained and he was transferred to the regional neurosurgical centre where magnetic resonance imaging revealed a contusion of the left half of the spinal cord adjacent to the 6th cervical vertebrae. Computed tomography revealed no bony injury but spinal column instability was demonstrated after flexion-extension spinal views and he underwent surgery to fuse his spine at the C5-C6 level. This report highlights the necessity to observe strict ATLS guidelines. This must include a thorough examination of the central and peripheral nervous system where spinal injury is suspected, even in the absence of radiographic abnormality and neck pain. This article also presents the unusual phenomena of Brown-Sequard syndrome and unilateral Horner's syndrome after blunt traumatic injury to the cervical spine.  (+info)

Isolated abducens nerve paresis associated with incomplete Horner's syndrome caused by petrous apex fracture--case report and anatomical study. (5/97)

A 17-year-old male presented with a wound on the right temporal region, oozing hemorrhagic necrotic brain tissue and cerebrospinal fluid, following a fall. Computed tomography showed temporoparietal and petrous apex fractures on the right. Neurological examination revealed abducens nerve paresis, ptosis, and myosis on the right side. The patient was treated surgically for the removal of the free bony fragments at the fracture site and to close the dural tear. The abducens nerve paresis, ptosis, and myosis persisted at the 3rd monthly postoperative follow-up examination. The anatomy of the abducens nerve at the petroclival region was studied in four cadaveric heads. Two silicone-injected heads were used for microsurgical dissections and two for histological sections. The abducens nerve has three different angulations in the petroclival region, located at the dural entrance porus, the petrous apex, and the lateral wall of the cavernous segment of the internal carotid artery. The abducens nerve had fine anastomoses with the trigeminal nerve and the periarterial sympathetic plexus. There were fibrous connections extending inside the venous space of the petroclival area. The abducens nerve seems to be vulnerable to damage in the petroclival region, either directly by trauma to its dural porus and petrous apex or indirectly by stretching of the nerve through the nervous and/or fibrous connections. Concurrent functional loss of the abducens nerve and the periarterial sympathetic plexus clinically manifested as incomplete Horner's syndrome in our patient.  (+info)

Agenesis of the internal carotid artery associated with aortic arch anomaly in a patient with congenital Horner's syndrome. (6/97)

We report a rare case of agenesis of the left internal carotid artery (ICA) and an aortic arch anomaly that presented with ipsilateral congenital Horner's syndrome. Digital subtraction angiography revealed left ICA agenesis shortly after its origin and anastomosis between the left maxillary artery and the supraclinoid segment of the left ICA. Aortography of the aortic arch revealed the right subclavian artery arising as the first branch of a left aortic arch, followed by a bicarotid trunk and a left subclavian artery. High resolution CT of the skull base revealed the absence of the left carotid channel, consistent with congenital agenesis of the ICA.  (+info)

Trigeminal and polyradiculoneuritis in a dog presenting with masticatory muscle atrophy and Horner's syndrome. (7/97)

A 9-year-old, spayed female, Airedale Terrier was euthanatized and necropsied after a progressive clinical course that included Horner's syndrome of the left eye and unilateral atrophy of the masticatory muscles. Although gross lesions were limited, a polyradiculoneuritis and ganglionitis that was most severe in the trigeminal nerves and ganglia were confirmed histologically. The inflammatory infiltrate consisted predominantly of macrophages and B and T lymphocytes that were phenotypically confirmed by immunostaining. Horner's syndrome was the result of damage to postganglionic sympathetic fibers that were incorporated in segments of the inflamed trigeminal nerve and its ophthalmic branch. Histologically, the character and distribution of the inflammation was similar to previously described syndromes of suspected immune-mediated etiology in humans and animals.  (+info)

Artemin is a vascular-derived neurotropic factor for developing sympathetic neurons. (8/97)

Artemin (ARTN) is a member of the GDNF family of ligands and signals through the Ret/GFRalpha3 receptor complex. Characterization of ARTN- and GFRalpha3-deficient mice revealed similar abnormalities in the migration and axonal projection pattern of the entire sympathetic nervous system. This resulted in abnormal innervation of target tissues and consequent cell death due to deficiencies of target-derived neurotrophic support. ARTN is expressed along blood vessels and in cells nearby to sympathetic axonal projections. In the developing vasculature, ARTN is expressed in smooth muscle cells of the vessels, and it acts as a guidance factor that encourages sympathetic fibers to follow blood vessels as they project toward their final target tissues. The chemoattractive properties of ARTN were confirmed by the demonstration that sympathetic neuroblasts migrate and project axons toward ARTN-soaked beads implanted into mouse embryos.  (+info)

Horner syndrome, also known as Horner's syndrome or oculosympathetic palsy, is a neurological disorder characterized by the interruption of sympathetic nerve pathways that innervate the head and neck, leading to a constellation of signs affecting the eye and face on one side of the body.

The classic triad of symptoms includes:

1. Ptosis (drooping) of the upper eyelid: This is due to the weakness or paralysis of the levator palpebrae superioris muscle, which is responsible for elevating the eyelid.
2. Miosis (pupillary constriction): The affected pupil becomes smaller in size compared to the other side, and it may not react as robustly to light.
3. Anhydrosis (decreased sweating): There is reduced or absent sweating on the ipsilateral (same side) of the face, particularly around the forehead and upper eyelid.

Horner syndrome can be caused by various underlying conditions, such as brainstem stroke, tumors, trauma, or certain medical disorders affecting the sympathetic nervous system. The diagnosis typically involves a thorough clinical examination, pharmacological testing, and sometimes imaging studies to identify the underlying cause. Treatment is directed towards managing the underlying condition responsible for Horner syndrome.

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.

Mydriasis is a medical term that refers to the dilation or enlargement of the pupil, which is the black circular opening in the center of the iris (the colored part) of the eye. The pupil normally adjusts its size in response to changes in light levels and emotional state. In mydriasis, the pupil becomes widely dilated and less responsive to light. This can occur naturally due to factors such as strong emotions, fear, or physical exertion, but it can also be caused by certain medications, eye drops, or medical conditions like brain injuries or neurological disorders. It is important to note that mydriasis can affect one or both eyes and may have different clinical significance depending on the context.

A carotid artery, internal, dissection is a medical condition that affects the internal carotid artery, which is a major blood vessel in the neck that supplies oxygenated blood to the brain. In this condition, there is a separation (dissection) of the layers of the artery wall, causing blood to accumulate in the space between the layers. This can lead to narrowing or blockage of the artery, reducing blood flow to the brain and increasing the risk of stroke. Internal carotid artery dissection can be caused by trauma, high blood pressure, connective tissue disorders, or spontaneously. Symptoms may include neck pain, headache, facial pain, visual disturbances, weakness or numbness in the arms or legs, difficulty speaking or understanding speech, and dizziness or loss of balance.

Anisocoria Harlequin syndrome "Horner syndrome: MedlinePlus Medical Encyclopedia". medlineplus.gov. Retrieved 2019-05-06. ... The syndrome is named after Johann Friedrich Horner, the Swiss ophthalmologist who first described the syndrome in 1869. ... on the affected side of Horner syndrome (the opposite effect to what the cocaine test would produce in the presence of Horner's ... "Isolated horner syndrome secondary to eagle syndrome". Neurology and Clinical Neuroscience. 7 (3): 156-157. doi:10.1111/ ...
This is a diagnostic test for Horner's syndrome. Patients with Horner's syndrome exhibit anisocoria brought about by lesions on ... Davagnanam I, Fraser CL, Miszkiel K, Daniel CS, Plant GT (March 2013). "Adult Horner's syndrome: a combined clinical, ... Walton KA, Buono LM (December 2003). "Horner syndrome". Current Opinion in Ophthalmology. 14 (6): 357-63. doi:10.1097/00055735- ...
Horner's syndrome is the disruption of a nerve pathway from the brain to the face and eye on one side of the body. This also ... Babinski-Nageotte's syndrome is often confused or associated with other syndromes. The syndromes being Reinhold syndrome ( ... hemimedullary syndrome) and Wallenberg syndrome. Although confused for one another they are different syndromes each with their ... Babinski-Nageotte syndrome is clinically distinct from Reinhold's syndrome (hemimedullary syndrome). This has led to confusion ...
Horner's syndrome may be associated. In the original description, the vagus and glossopharyngeal nerves were involved; ... Avellis syndrome is a neurological disorder characterized by a peculiar form of alternating paralysis. There is paralysis of ... "Avellis Syndrome". whonamedit. Retrieved 10 Mar 2013. (Articles with short description, Short description matches Wikidata, ... Krasnianski, M; Neudecker, S; Schlüter, A; Zierz, S (Dec 2003). "Avellis' Syndrome in Brainstem Infarctions". Fortsch. Neurol. ...
This is seen in Horner's syndrome. The ptosis seen in Horner's syndrome is of a lesser degree than is seen with an oculomotor ...
Horner syndrome, another problem associated with the sympathetic nervous system, is often seen in conjunction with harlequin ... Horner's syndrome NIH - National Cancer Institute. "Autonomic Nervous System". PubMed Health. Lance, J. W. (2005). "Harlequin ... Harlequin syndrome affects fewer than 1000 people in the United States. Symptoms associated with Harlequin syndrome are more ... Since the cause and mechanism of Harlequin syndrome is still unknown, there is no way to prevent this syndrome. Although the ...
This test can also reveal Horner's syndrome. Minor, Victor (1928). "Ein neues Verfahren zu der klinischen Untersuchung der ... Objective Demonstration of Horner's Syndrome". Indian Journal of Otolaryngology and Head & Neck Surgery. 67 (2): 190-192. doi: ...
Horner's syndrome "ciliospinal centre from Online Medical Dictionary". Retrieved 2007-06-05. Patestas, Maria A.; Gartner, ...
... and Horner's syndrome by disrupting the sympathetic nervous system. Horner's syndrome is also common in tumors at the top of ... Tumors obstructing bloodflow to the heart can cause superior vena cava syndrome (swelling of the upper body and shortness of ... Lung tumors often cause the release of body-altering hormones, which cause unusual symptoms, called paraneoplastic syndromes. ... Paraneoplastic syndromes involving the skin and kidneys are rare, each occurring in up to 1% of those with lung cancer. A ...
... may be useful in the diagnosis of Horner's syndrome. In Horner's syndrome, the sympathetic innervation to the ... Garibaldi DC, Hindman HB, Grant MP, Iliff NT, Merbs SL (2006). "Effect of 0.5% apraclonidine on ptosis in Horner syndrome". ... cocaine in the diagnosis of horner syndrome in pediatric patients". Journal of Ocular Pharmacology and Therapeutics. 22 (3): ... This causes the reversal of anisocoria that is characteristic of Horner's. Topical apraclonidine can also decrease IOP in ...
Compression of the sympathetic chain may cause Horner's syndrome. Many vertebrates, especially reptiles, have cervical ribs as ... The presence of a cervical rib can cause a form of thoracic outlet syndrome due to compression of the lower trunk of the ... Giles, Lynton G. F. (2009-01-01), Giles, Lynton G. F. (ed.), "Case 67 - Cervical ribs", 100 Challenging Spinal Pain Syndrome ... they may cause problems such as contributing to thoracic outlet syndrome, because of pressure on the nerves that may be caused ...
Lesions of the hypothalamospinal tract cause ipsilateral Horner's syndrome. Haines, Duane E. (January 2013). Fundamental ...
Collectively, these signs are referred to as Horner's syndrome. Other ocular abnormalities include ophthalmoplegia (paralysis ... Gorlin RJ, Cohen MM, Hennekam R (2001). "Chapter 24: Syndromes with unusual facies: well-known syndromes". Syndromes of the ... Syndromes affecting the skin, Syndromes affecting the nervous system, Diseases named for discoverer). ... The syndrome has a higher prevalence in females and typically appears between 5 and 15 years of age. In addition to the ...
... and Horner's syndrome from the involvement of sympathetic nerves. Involvement of the facial nerve is rare. As the guttural ...
... lesions of this area canonically lead to ipsilateral Horner's syndrome. Standring, Susan (2020). Gray's Anatomy: The Anatomical ...
Horner's syndrome may occur if nearby sympathetic fibers are involved.[citation needed] Tumors found in the external third of ...
Compression of the sympathetic chain may result in Horner's syndrome. Graves' ophthalmopathy (protrusion of one or both eyes) ... Anxiety syndromes related to hyperthyroidism are typically complicated by major depression and cognitive decline, such as in ... 2005;140(1) 49; Compression syndromes caused by substernal goitres. Anders HJ, Postgrad Med J. 1998;74(872) 327. "Graves' ...
Damage to the lateral column can result in Horner's syndrome. Multiple system atrophy (MSA), has also been linked to the ...
Congenital Horner's syndrome - sometimes inherited, although usually acquired. Waardenburg syndrome - a syndrome in which ... Acquired Horner's syndrome - usually acquired, as in neuroblastoma, although sometimes inherited. Neoplasm - Melanomas can also ... Parry-Romberg syndrome - due to tissue loss. Heterochromia has also been observed in those with Duane syndrome. Chronic iritis ... Iridocorneal endothelium syndrome Iris ectropion syndrome Fuchs heterochromic iridocyclitis - a condition characterized by a ...
Enophthalmos in Horner's syndrome is an illusion created by the subtle ptosis of the upper eyelid caused by paralysis of the ... Horner's syndrome causes paralysis of the structures of the eye and orbit that receive sympathetic innervation. The signs of ... While some attribute the enophthalmos of Horner's Syndrome to paralysis of the orbitalis muscle, this is inaccurate. ... Horner's syndrome are ptosis, miosis, anhydrosis, and (apparent) enophthalmos. ...
Horner's syndrome* results from damage to the sympathetic innervation of the eye. Signs include enophthalmos (sunken eye), ... Dermal fragility syndrome, also known as Ehlers-Danlos-like syndrome, is a rare condition in dogs characterized by increased ... White dog shaker syndrome causes full body tremors in small, white dog breeds. It is most common in West Highland White ... Legg-Calvé-Perthes syndrome, also known as Perthes disease or avascular necrosis of the femoral head, is characterized by a ...
... is the abnormal pupil and suggests Horner's syndrome or mechanical anisocoria. In Horner's syndrome sympathetic nerve fibers ... This is because Horner's syndrome and oculomotor nerve lesions both cause ptosis. Anisocoria is usually a benign finding, ... Horner's syndrome Mechanical anisocoria: Occasionally previous trauma, eye surgery, or inflammation (uveitis, angle closure ... Some of the causes of anisocoria are life-threatening, including Horner's syndrome (which may be due to carotid artery ...
If Horner syndrome is present, there is miosis (constriction of the pupils) in the affected eye.[citation needed] The injury ... Involvement of T1 may result in Horner's syndrome, with ptosis, and miosis. Weakness or lack of ability to use specific muscles ... Huang YG, Chen L, Gu YD, Yu GR (May 2008). "Histopathological basis of Horner's syndrome in obstetric brachial plexus palsy ... ISBN 978-0-8016-3227-3. pp.576, 667 Page 512: Lower Radicular Syndrome (Klumpke Paralysis) in: Pedley, Timothy A.; Rowland, ...
February 1995). "Pholedrine: a substitute for hydroxyamphetamine as a diagnostic eyedrop test in Horner's syndrome". Journal of ... is administered as a topical eye drop form for the purpose of dilating the pupil and can be used to diagnose Horner's syndrome ...
A Pancoast tumor can give rise to both Pancoast syndrome and Horner's syndrome. When the brachial plexus roots are involved, it ... resulting in a range of symptoms known as Horner's syndrome. Pancoast tumors are named for Henry Pancoast, an American ... Pancoast tumor can include a complete Horner's syndrome in severe cases: miosis (constriction of the pupils), anhidrosis (lack ... of sympathetic fibers as they exit the cord at T1 and ascend to the superior cervical ganglion will produce Horner's syndrome.[ ...
Horner's syndrome, Marcus Gunn jaw winking syndrome and third cranial nerve misdirection. Myogenic ptosis, which includes ... When caused by Horner's syndrome, ptosis is usually accompanied by miosis and anhidrosis. In this case, the ptosis is due to ... Acquired Horner syndrome may result after trauma, neoplastic insult or even vascular disease. Ptosis caused by trauma can ensue ... Congenital neurogenic ptosis is believed to be caused by Horner's syndrome, in which a mild ptosis may be associated with ...
Horner's syndrome is a disorder resulting from damage to the sympathetic autonomic nervous pathway in the head. Damage to the ... often results in Horner's syndrome. Damage to the T1-T3 regions of the spinal cord is responsible for drooping of the eyelids ( ... see Horner's Syndrome: Pathophysiology). Familial dysautonomia is a genetic disorder characterized by abnormalities of sensory ...
Complications of cerebrovascular FMD include TIA, ischemic stroke, Horner syndrome, or subarachnoid hemorrhage. Patients with ... The vascular subtype of Ehlers-Danlos Syndrome (type IV) has been associated with multi-focal FMD. This syndrome should be ... The differentiating presentations are suggestive of FMD being a unique syndrome in respect to the pediatric population. ... FMD present in the subclavian artery may cause arm weakness, paresthesia, claudication, and subclavial steal syndrome. Children ...
However, if accompanied by ptosis of the upper eyelid, this may indicate Horner's syndrome. If there is a small, irregular ...
This reflex is absent in Horner's syndrome and lesions involving the cervical sympathetic fibers. The enhanced ciliospinal ...
Anisocoria Harlequin syndrome "Horner syndrome: MedlinePlus Medical Encyclopedia". medlineplus.gov. Retrieved 2019-05-06. ... The syndrome is named after Johann Friedrich Horner, the Swiss ophthalmologist who first described the syndrome in 1869. ... on the affected side of Horner syndrome (the opposite effect to what the cocaine test would produce in the presence of Horners ... "Isolated horner syndrome secondary to eagle syndrome". Neurology and Clinical Neuroscience. 7 (3): 156-157. doi:10.1111/ ...
Horners syndrome) results from an interruption of the sympathetic nerve supply to the eye and is characterized by the classic ... The term Horner syndrome is commonly used in English-speaking countries, whereas the term Ber... ... whereas the term Bernard-Horner syndrome is common in France. Von Passow syndrome is an association of Horner syndrome with ... Treatment of Horner Syndrome. In general, appropriate treatment of Horner syndrome depends on the underlying cause. The goal of ...
Horners syndrome and ipsilateral tongue paresis due to carotid artery dissection Message subject: (Your Name) has forwarded a ...
A case of Brown-Sequard syndrome with associated Horners syndrome after blunt injury to the cervical spine ... This article also presents the unusual phenomena of Brown-Sequard syndrome and unilateral Horners syndrome after blunt ... A case of Brown-Sequard syndrome with associated Horners syndrome after blunt injury to the cervical spine ... and a Brown-Sequard syndrome, with a sensory level at C6. Immobilisation was maintained and he was transferred to the regional ...
... syndrome secondary to invasive Blastomyces pneumonia and provide a review of the rare infectious etiologies of this syndrome. ... and 7 cases of the parasite Echinococcus causing infectious Horner syndrome (4). Infectious causes of Horner syndrome have even ... An unusual cause of Horner syndrome. J Gen Intern Med. 2018;33:774-5. [PMID: 29383548] doi:10.1007/s11606-018-4317-x Crossref ... His Horner syndrome resolved during this same period. He regained ability to ambulate and had no residual neurologic deficits. ...
The medical records of 74 dogs and 26 cats with Horners syndrome (HS) that were admitted to the New York State College of ... The medical records of 74 dogs and 26 cats with Horners syndrome (HS) that were admitted to the New York State College of ...
Horner Syndrome - Etiology, pathophysiology, symptoms, signs, diagnosis & prognosis from the MSD Manuals - Medical Professional ... Etiology of Horner Syndrome Horner syndrome results when the cervical sympathetic pathway running from the hypothalamus to the ... Symptoms and Signs of Horner Syndrome Symptoms of Horner syndrome include ptosis, miosis, anhidrosis, and hyperemia of the ... The cause of Horner syndrome, if identified, is treated; there is no treatment for primary Horner syndrome. ...
... (HS) is a neurological disorder characterized by a symptom triad of miosis (an abnormally small pupil), partial ... Triad of Horner syndrome * Miosis (constriction of the pupil) *Occurs because the sympathetically controlled iris dilator ... Horner syndrome: clinical perspectives. . Eye and Brain. 2015. : p.35. .doi:. 10.2147/eb.s63633. .. ,. Open in Read by QxMD ... Remember the symptoms of Horner syndrome by the great HORNs of the PAMpas deer: Ptosis, Anhidrosis, and Miosis. ...
Horner syndrome answers are found in the Tabers Medical Dictionary powered by Unbound Medicine. Available for iPhone, iPad, ... "Horner Syndrome." Tabers Medical Dictionary, 24th ed., F.A. Davis Company, 2021. Nursing Central, nursing.unboundmedicine.com/ ... nursingcentral/view/Tabers-Dictionary/760821/0/Horner_syndrome. Horner syndrome. In: Venes DD, ed. Tabers Medical Dictionary. ... Horner Syndrome [Internet]. In: Venes DD, editors. Tabers Medical Dictionary. F.A. Davis Company; 2021. [cited 2023 December ...
Horners syndrome is a common disorder of a sudden loss of stimulation of the nerves-of the eyes and area surrounding the eyes. ... Horners syndrome is caused when the nervous system gets damaged and stops functioning in the eye, ear, or neck area. ... Treatment is not necessary for horners syndrome because it usually resolves on its own in a few weeks. However, any underlying ... This syndrome is just a cosmetic issue-it does not cause pain, and does not affect vision. ...
There is a chance of having Horners syndrome due to congenital abnormality. Read on to know more. ... Is Horners Syndrome Hereditary & How Does Lung Cancer Cause It?. *What Nerve Is Involved In Horners Syndrome & What Cranial ... Is Horners Syndrome A Serious Condition & Can It Be Reversed?. *What Is The Prognosis For Horners Syndrome & Lifestyle ... Prevention From Horners Syndrome. Yes, it is possible to prevent congenital Horners syndrome. Prevention can be possible by ...
"Iatrogenic Horners Syndrome: A Complication of Thoracostomy-Tube Replacement",. abstract = "To the Editor: Horners syndrome ... Iatrogenic Horners Syndrome: A Complication of Thoracostomy-Tube Replacement. / Kahn, Sarah A.; Brandt, Larry J. In: New ... Iatrogenic Horners Syndrome: A Complication of Thoracostomy-Tube Replacement. New England Journal of Medicine. 1985 Jan 24;312 ... To the Editor: Horners syndrome consists of ptosis, meiosis, and anhidrosis and may result from any lesion that interrupts the ...
Horners syndrome may be congenital or acquired.. *Congenital: Horners syndrome is present at birth in a small percentage of ... How is Horners syndrome diagnosed?. The diagnosis of Horners syndrome may be complex, since other disorders may cause similar ... How is Horners syndrome treated?. The treatment will depend on which kind of underlying disorder is causing Horners syndrome ... Horners syndrome, also known as oculosympathetic palsy or Bernard-Horner syndrome, is a relatively rare condition that affects ...
Horner syndrome. The presence of a lesion at any point along the oculosympathetic pathway results in Horner syndrome, which is ... Congenital Horner syndrome is usually caused by birth trauma to the brachial plexus. Nontraumatic Horner syndrome in infants ... Horner syndrome associated with pain deserves special attention. Painful postganglionic Horner syndrome is a distinct clinical ... may also cause painful Horner syndrome during an acute attack (see Chapter 12). The Horner syndrome often resolves but may ...
The cause of Horners syndrome is an interruption of the sympathetic ... Horners syndrome causes a droopy lid and smaller pupil on one side of the face. ... Horners syndrome causes a droopy lid and smaller pupil on one side of the face. The cause of Horners syndrome is an ... How is Horners syndrome diagnosed?. Eye drops are often used to diagnose this condition. The two findings of a Horners ...
Horners syndrome classically presents with anhidrosis, ptosis, miosis, and enophthalmos. The simple mnemonic, SAMPLE can be ... A simple Horner syndrome mnemonic is SAMPLE.. *Syringomyelia, Spinal trauma above the T2 spinal level, Spinal cord tumors and S ... How does thyromegaly cause Horner Syndrome?. The superior cervical ganglion (SCG) serves as a relay center for higher-order ... Horners syndrome classically presents with anhidrosis, ptosis, miosis, and enophthalmos. The simple mnemonic, SAMPLE can be ...
How common is Horner syndrome?. About 1 in 6,250 babies are born with Horner syndrome. The incidence of Horner syndrome that ... Horner syndrome that appears after the newborn period (acquired Horner syndrome) and most cases of congenital Horner syndrome ... Acquired Horner syndrome and most cases of congenital Horner syndrome have non-genetic causes. Rarely, congenital Horner ... What is Horner syndrome?. Horner syndrome is a disorder that affects the eye and surrounding tissues on one side of the face ...
Horners Syndrome: Awareness, Action & Advocacy Foundation. Horners Syndrome: Awareness, Action & Advocacy FoundationHorners ... Horners Syndrome: Awareness, Action & Advocacy Foundation. Horners Syndrome: Awareness, Action & Advocacy FoundationHorners ... The best way to start is to clarify what is not Horners Syndrome. Horners Syndrome is not pink eye. According to the Genetic ... Horner syndrome: What causes it?. MayoClinic.com. May 06, 2014; http://www.mayoclinic.org/diseases-conditions/horner-syndrome/ ...
Horners) Syndrome - Causes, Treatment, Symptoms in Dogs, Cat. It is a mainly eye related disorder of sympathetic nerve fibers ... What is Horners Syndrome?. Horners syndrome is a mainly eye related disorder, comparatively rare development. This disorder ... The idiopathic incidence is common in Horner syndrome, but medical researchers also found that some of the Horner syndrome ... patient.info/in/doctor/horners-syndrome. *Horners Syndrome (2003); National Organization for Rare disorders; Retrieve from: ...
Horners syndrome in a cat. This cat has a normal eye on the cats right, and an eye with Horners syndrome on the cats left. ... The most important thing is to determine what caused the Horners syndrome. The Horners syndrome itself probably does not need ... It is not necessary to treat Horners syndrome. The syndrome is not painful and does not interfere with vision. The ... Horners syndrome stemming from any injury such as one of these might prompt a search for other neurologic issues. Advanced ...
... system of the neck particularly in a high-risk woman with presentation of dysphagia and manifestations of Horners syndrome. ... Esophageal involvement and Horners syndrome are rare manifestations of breast cancer distant metastases that can pose a ... described Horners syndrome resulting from malignant pleural effusion in metastatic breast cancer [5]. Vitale et al. reported ... Unusual Horners syndrome in recurrent breast cancer: evaluation using 18F-FDG PET/CT. Nucl Med Mol Imaging. 2017;51:93-6. ...
... recurrent laryngeal nerves or Horners syndrome [1,2]. Horners Syndrome consists of the set of signs and symptoms which ... Transient Ipsilateral Horners Syndrome after Ultrasound Guided Interscalene Brachial Plexus Nerve Block Monica Yadav, MD1, ... The above clinical triad was suggestive of Horners syndrome. The patient was observed in preoperative area and symptoms ... Schwalbert A, de PaduaResende Filho D (2021) 189 A case of horners syndrome after ultrassom-guided interscalene brachial ...
Pancoast syndrome will develop when the brachial roots of the brachial plantar plexus are affected. The sympathetic fibers that ... exit the cord at T1 will ascend to the superior cervical glandlion and will be involved in the formation of Horners syndrome. ... How does lung cancer cause Horners syndrome? Carcinomas in the superior pulmonary sulcus produce Pancoast syndrome, thus ... What causes Pancoast tumor Horners syndrome and how can it be prevented? Pancoast tumors are a type of apical tumor and they ...
Neurology Section 17 - Spinal Cord Diseases: Poliomyelitis, Amyotrophic Lateral Sclerosis & Horner Syndrome. This content is ...
B. Horners Syndrome Explanation. Horners Syndrome refers to a pupil abnormality characterized by a unilateral, small, regular ... Horners Syndrome is characterized by a small, constricted pupil and other symptoms like drooping eyelid and decreased sweating ... Argyll Robertson Pupil and Horners Syndrome are both conditions that can cause abnormal pupillary responses, but they are not ... Horners syndrome). It is a positional defect that gives the person a sleepy appearance and impairs vision.. *. A. ...
This article delves into the intricate world of Horners Syndrome, exploring its causes, symptoms, and available treatment ... Horners Syndrome is a complex neurological condition that manifests through a distinct set of symptoms, primarily affecting ... Horners Syndrome is a complex neurological condition that manifests through a distinct set of symptoms, primarily affecting ... Unlike Horners Syndrome, in which the affected pupil is smaller, reverse Horners Syndrome involves a larger pupil on the ...
... ... 7. Lebas M, Seror J, Debroucker T. Positive apraclonidine test 36 hours after acute onset of horner syndrome in dorsolateral ... Superior oblique paresis and contralateral Horners syndrome. Ann Ophthalmol 1983; 15:681-683. 4. Bazan R, Braga GP, Gomes DL, ... Trochlear nerve palsy associated with claude bernard-horner syndrome after brainstem stroke. Case Rep Neurol 2011; 3: 248-251. ...
acquired Horners syndrome. *ocular melanosis. *iris tumor. *Posner-Schlossman syndrome. *Chediak-Higashi syndrome ...
Horner Syndrome. * Lyme Disease. * Marcus Gunn Jaw-winking Syndrome. * Multiple Sclerosis. * Neuro-ophthalmic History ...

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