Familial hemiplegic migraine (FHM) is an autosomal dominant type of hemiplegic migraine that typically includes weakness of half the body which can last...

can run in the family, called familial hemiplegic migraine, or in a single individual, called sporadic hemiplegic migraine. The symptoms can be similar...

headache. Two other varieties are familial hemiplegic migraine and sporadic hemiplegic migraine, in which a person has migraine with aura and with accompanying...

profound vestibular loss. The syndrome responds to acetazolamide. Familial hemiplegic migraine (FHM) has been linked to mutations in the calcium channel gene...

Retinal migraine is a retinal disease often accompanied by migraine headache and typically affects only one eye. It is caused by ischaemia or vascular...

vertebrobasilar territory to restore normal brainstem function. Familial hemiplegic migraine (FHM) is migraine with a possible polygenetic cause—in fact, FHM can only...

of migraine. Sporadic hemiplegic migraine (SHM) has clinical symptoms identical to familial hemiplegic migraine (FHM) and distinct from migraine with...

patients with EA also have migraine or progressive cerebellar degenerative disorders, symptomatic of either familial hemiplegic migraine or spinocerebellar ataxia...

neuronal death in energy-compromised tissue. CSD has also been implicated in migraine aura, where CSD is assumed to ascend in well-nourished tissue and is typically...

(July 31, 2012). "Familial PRRT2 mutation with heterogeneous paroxysmal disorders including paroxysmal torticollis and hemiplegic migraine". Developmental...

been associated with various neurologic disorders, including familial hemiplegic migraine, episodic ataxia type 2, and spinocerebellar ataxia type 6. "Voltage-dependent...

forms of familial hemiplegic migraine (FHM) has also been found. Benign familial infantile epilepsy is not genetically related to benign familial neonatal...

gene disorders that result in migraines are rare. One of these is known as familial hemiplegic migraine, a type of migraine with aura, which is inherited...

cerebrovascular dysfunction. The disorder most closely related to AHC is familial hemiplegic migraine which is caused by a mutation in a gene for calcium channel receptors...

Still others present with symptoms common to both SCA6 and familial hemiplegic migraine.[citation needed] Most cases of SCA6 are a result of CAG repeat...

S2CID 375183. Russell MB, Ducros A (May 2011). "Sporadic and familial hemiplegic migraine: pathophysiological mechanisms, clinical characteristics, diagnosis...

medication more than twice per week; and uncommon migraine conditions (e.g., hemiplegic migraine, migraine with prolonged aura, migrainous infarction). Patient...

episodic ataxia type 2 or familial hemiplegic migraine. Nearly all cases are caused by de novo mutations, though familial cases have been observed due...

ganglion neurons and are believed to be a main contributor to familial hemiplegic migraine. By using a knockin experiment, this mutation could be expressed...

the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine". Annals of Neurology. 49 (6): 753–760. doi:10.1002/ana.1031...

et al. (June 2004). "Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation". Annals of Neurology. 55 (6): 884–7...

tonic-clonic seizures (ICEGTC), Panayiotopoulos syndrome, familial hemiplegic migraine (FHM), familial autism, Rasmussens's encephalitis and Lennox-Gastaut...

University with a dissertation titled "The molecular basis of familial hemiplegic migraine". "Roel Ophoff". Catalogus Professorum. Retrieved 3 January 2021...

Calcium channel, voltage-dependent, P/Q type, alpha 1A subunit (Familial hemiplegic migraine Type I). Gene map locus 19p13 COMP: Cartilage oligomeric matrix...

epilepsy with febrile seizures plus Voltage-gated sodium channel Familial hemiplegic migraine various Associated with one particular disabling form of fibromyalgia...

tonic-clonic seizures (ICEGTC), Panayiotopoulos syndrome, familial hemiplegic migraine (FHM), familial autism, Rasmussens's encephalitis and Lennox-Gastaut...

provoked by stress, startle, or heavy exertion such as exercise. Familial hemiplegic migraine (FHM) Spinocerebellar ataxia type 13 Long QT syndrome is a ventricular...

hemiplegia of childhood Weber's syndrome Medial medullary syndrome Familial hemiplegic migraine Brain stem stroke syndrome "Alternating Hemiplegia Information...

other loci were observed such as the familial hemiplegic migraine (FHM) locus on chromosome 19p, or the familial infantile convulsions and paroxysmal...

PMID 11823106. S2CID 25555020. GeneReviews/NCBI/NIH/UW entry on Familial Hemiplegic Migraine GeneReviews/NCBI/NIH/UW entry on SCN1A-Related Seizure Disorders...