The ATP1A2 Mutation Associated with Hemiplegic Migraines: Case Report and Literature Review
Familial hemiplegic migraine type 2 is a premonitory subtype of migraine caused by an ATP1A2 gene mutation. It is an autosomal dominant genetic disease. Here, we report a 51-year-old woman who had a migraine attack due to a pathogenic ATP1A2 gene mutation. With frequent attacks, the patient develope...
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| Autori principali: | , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
MDPI AG
2022-11-01
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| Serie: | Clinical and Translational Neuroscience |
| Soggetti: | |
| Accesso online: | https://www.mdpi.com/2514-183X/6/4/25 |
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