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Hemiplegic migraine, familial type 2 MeSH Supplementary Concept Data 2024


MeSH Supplementary
Hemiplegic migraine, familial type 2
Unique ID
C537246
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C537246
Entry Term(s)
Familial hemiplegic migraine, type 2
Migraine, familial hemiplegic, 2
Registry Number
0
Heading Mapped to
*Migraine with Aura
Frequency
32
Note
An autosomal dominant type of familial hemiplegic migraine (Migraine with Aura) with onset between 6 to 30 years and characterized by hemiparesis or paresthesias, aphasia, headaches, and behavioral changes, with subsequent loss of consciousness. Mutations in the ATP1A2 gene have been identified. OMIM: 602481
Date of Entry
2010/08/25
Revision Date
2015/09/26
Hemiplegic migraine, familial type 2 Preferred
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