Searching for Familial Hemiplegic Migraine Support information? Find all needed info by using official links provided below.
https://rarediseases.info.nih.gov/diseases/10975/familial-hemiplegic-migraine
Jan 02, 2019 · The Migraine Trust, a support organization, offers information on Familial hemiplegic migraine In-Depth Information GeneReviews provides current, expert-authored, peer-reviewed, full-text articles describing the application of genetic testing to the diagnosis, management, and genetic counseling of patients with specific inherited conditions.
https://rarediseases.info.nih.gov/diseases/10768/hemiplegic-migraine
43 rows · Nov 17, 2014 · Hemiplegic migraine (HM) is a rare type of migraine with aura that occurs …
https://ghr.nlm.nih.gov/condition/familial-hemiplegic-migraine
Oct 29, 2019 · Familial hemiplegic migraine is a form of migraine headache that runs in families. Migraines usually cause intense, throbbing pain in one area of the head, often accompanied by nausea, vomiting, and extreme sensitivity to light and sound.
https://www.diseaseinfosearch.org/Familial+Hemiplegic+Migraine/9656/support
Familial Hemiplegic Migraine - Disease Support - find support groups and organizations Are you looking for disease information or support? Simply type in the name of a disease or condition and Disease InfoSearch will locate quality information from a database of more than 13,000 diseases and thousands of support groups and foundations.
https://rarediseases.org/rare-diseases/hemiplegic-migraine/
Some individuals have familial hemiplegic migraine but do not have variations in these genes. Researchers believe that there are additional gene or genes that cause this disorder, but that have yet to be identified. Some researchers believe that variations in the PRRT2 gene may also cause familial hemiplegic migraine, but this theory is ...
https://www.ambrygen.com/clinician/genetic-testing/120/neurology/familial-hemiplegic-migraine
Familial hemiplegic migraine (FHM) is a hereditary form of migraine with aura. Confirmation of a diagnosis of FHM through genetic testing may guide medical treatment and management, as well as inform testing of family members.
https://en.wikipedia.org/wiki/Hemiplegic_migraine,_familial
Familial hemiplegic migraine (FHM) is an autosomal dominant type of hemiplegic migraine that typically includes weakness of half the body which can last for hours, days, or weeks. It can be accompanied by other symptoms, such as ataxia, coma, and paralysis. Migraine attacks may be provoked by minor head trauma.Specialty: Neurology
https://migraine.com/migraine-types/familial-hemiplegic-migraine/
Familial hemiplegic migraine is the form of HM in which this family link can be established, whereas HM that occurs without evidence of this genetic connection is called sporadic hemiplegic migraine. FHM is a very rare condition: it is estimated to occur in only about 0.01% of the population. According to a 2002 study of FHM in Denmark with 147 ...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3702875/
Familial hemiplegic migraine is a rare subtype of migraine with aura which includes motor weakness. A 32-year-old woman with known familial hemiplegic migraine (point mutation in Exon 22 of the ATP1A2 gene) presented with an acute confusional state, after an initially typical migraine. On ...Cited by: 4
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