Childhood-onset of recurrent headaches with an oculomotor cranial nerve palsy. Typically, ABDUCENS NERVE; OCULOMOTOR NERVE; and TROCHLEAR NERVE are involved with DIPLOPIA and BLEPHAROPTOSIS.
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.
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.
A class of disabling primary headache disorders, characterized by recurrent unilateral pulsatile headaches. The two major subtypes are common migraine (without aura) and classic migraine (with aura or neurological symptoms). (International Classification of Headache Disorders, 2nd ed. Cephalalgia 2004: suppl 1)
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 subtype of migraine disorder, characterized by recurrent attacks of reversible neurological symptoms (aura) that precede or accompany the headache. Aura may include a combination of sensory disturbances, such as blurred VISION; HALLUCINATIONS; VERTIGO; NUMBNESS; and difficulty in concentrating and speaking. Aura is usually followed by features of the COMMON MIGRAINE, such as PHOTOPHOBIA; PHONOPHOBIA; and NAUSEA. (International Classification of Headache Disorders, 2nd ed. Cephalalgia 2004: suppl 1)
Recurrent unilateral pulsatile headaches, not preceded or accompanied by an aura, in attacks lasting 4-72 hours. It is characterized by PAIN of moderate to severe intensity; aggravated by physical activity; and associated with NAUSEA and / or PHOTOPHOBIA and PHONOPHOBIA. (International Classification of Headache Disorders, 2nd ed. Cephalalgia 2004: suppl 1)

Ophthalmoplegic "migraine" or recurrent ophthalmoplegic cranial neuropathy: new cases and a systematic review. (1/2)

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Adult-onset migraine-related ophthalmoplegia and omolateral fetal-type posterior cerebral artery. (2/2)

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'Ophthalmoplegic migraine' is a term that was previously used to describe a condition characterized by headaches associated with one-sided paralysis of the nerves that control eye movement (ophthalmoplegia). This results in drooping of the eyelid, double vision, and pupil dilation on the affected side.

However, it's important to note that 'ophthalmoplegic migraine' is no longer considered a valid diagnosis by the International Headache Society (IHS) due to lack of clear understanding of its underlying pathophysiology. Instead, such cases are now more likely to be classified under other headache disorders, such as "migraine with brainstem aura" or "recurrent painful ophthalmoplegic neuropathy," depending on the specific symptoms and clinical presentation.

Therefore, it's best to consult with a healthcare professional for an accurate diagnosis and appropriate treatment plan based on the individual's symptoms and medical history.

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 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.

A migraine disorder is a neurological condition characterized by recurrent headaches that often involve one side of the head and are accompanied by various symptoms such as nausea, vomiting, sensitivity to light and sound, and visual disturbances. Migraines can last from several hours to days and can be severely debilitating. The exact cause of migraines is not fully understood, but they are believed to result from a combination of genetic and environmental factors that affect the brain and blood vessels. There are different types of migraines, including migraine without aura, migraine with aura, chronic migraine, and others, each with its own specific set of symptoms and diagnostic criteria. Treatment typically involves a combination of lifestyle changes, medications, and behavioral therapies to manage symptoms and prevent future attacks.

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.

"Migraine with Aura" is a neurological condition that is formally defined by the International Classification of Headache Disorders (ICHD) as follows:

"An migraine attack with focal neurological symptoms that usually develop gradually over 5 to 20 minutes and last for less than 60 minutes. Motor weakness is not a feature of the aura."

The symptoms of an aura may include visual disturbances such as flickering lights, zigzag lines, or blind spots; sensory disturbances such as tingling or numbness in the face, arms, or legs; and speech or language difficulties. These symptoms are caused by abnormal electrical activity in the brain and typically precede or accompany a migraine headache, although they can also occur without a headache.

It's important to note that not all people who experience migraines will have an aura, and some people may have an aura without a headache. If you are experiencing symptoms of a migraine with aura or any other type of headache, it is recommended that you consult with a healthcare professional for proper diagnosis and treatment.

"Migraine without Aura," also known as "Common Migraine," is defined by the International Classification of Headache Disorders (ICHD-3) as follows:

"Headaches fulfilling criteria C and D:

C. At least five attacks fulfilling criterion B

B. Headache lasting 4-72 hours (untreated or unsuccessfully treated)

1. a) Has at least two of the following characteristics:
b) One-sided location
c) Pulsating quality
d) Moderate or severe pain intensity
e) Aggravation by or causing avoidance of routine physical activity (e.g., walking or climbing stairs)

D. During headache at least one of the following:

1. a) Nausea and/or vomiting
2. b) Photophobia and phonophobia"

In simpler terms, Migraine without Aura is a recurring headache disorder characterized by moderate to severe headaches that typically occur on one side of the head, have a pulsating quality, and are aggravated by physical activity. The headaches last between 4 and 72 hours if not treated or if treatment is unsuccessful. Additionally, during the headache, at least one of the following symptoms must be present: nausea/vomiting, sensitivity to light (photophobia), or sensitivity to sound (phonophobia).

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Ophthalmoplegic migraine. Daroff RB. Daroff RB. Cephalalgia. 2001 Mar;21(2):81. doi: 10.1046/j.1468-2982.2001.00174.x. ... MR imaging of migraine. Prager J, Rosenblum J. Prager J, et al. AJNR Am J Neuroradiol. 1991 Nov-Dec;12(6):1268. AJNR Am J ... Imaging findings of migraine. Cutrer FM, Black DF. Cutrer FM, et al. Headache. 2006 Jul-Aug;46(7):1095-107. doi: 10.1111/j.1526 ... Migraine mimics. Evans RW. Evans RW. Headache. 2015 Feb;55(2):313-22. doi: 10.1111/head.12518. Epub 2015 Feb 6. Headache. 2015. ...
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Recurrent painful ophthalmoplegic neuropathy (RPON), previously known as ophthalmoplegic migraine (OM), is a rare neurological ... Carlow, Thomas J. (Sep 2002). "Oculomotor Ophthalmoplegic Migraine: Is It Really Migraine?". Journal of Neuro-Ophthalmology. 22 ... "Ophthalmoplegic Migraine: Inflammatory Neuropathy with Secondary Migraine?". Canadian Journal of Neurological Sciences / ... "Ophthalmoplegic migraine: Migraine or oculomotor neuropathy?". Cephalalgia. 32 (16): 1208-1215. doi:10.1177/0333102412463493. ...
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B1 Ophthalmoplegic migraine, intractable Ophthalmoplegic migraine, with refractory migraine G43. However, no other theoretical ...
Hemiplegic migraine, familial, see Familial hemiplegic migraine. *Hemiplegic-ophthalmoplegic migraine, see Familial hemiplegic ...
Lane R, Davies P. Ophthalmoplegic migraine: the case for reclassification. Cephalalgia. 2010 Jun. 30(6):655-61. [QxMD MEDLINE ... Migraine, Tolosa-Hunt syndrome and pleocytosis. Correlation or coincidence?. Clin Neurol Neurosurg. 1984. 86(1):33-41. [QxMD ...
Ophthalmoplegic Migraine Syndrome Previous Indexing. Migraine Disorders (1964-2011). Ophthalmoplegia (1964-2011). Public MeSH ... Ophthalmoplegic Migraine Preferred Term Term UI T784943. Date02/01/2011. LexicalTag NON. ThesaurusID NLM (2012). ... Ophthalmoplegic Migraine Syndrome Term UI T784944. Date02/01/2011. LexicalTag NON. ThesaurusID NLM (2012). ... Ophthalmoplegic Migraine. Tree Number(s). C10.228.140.546.399.750.725. C10.292.562.750.375. C10.292.675. C10.314.687. C10.597. ...
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