Familial hemiplegic migraine type 2: a case report of an adolescent with ATP1A2 mutation
This study presents a case report of a male adolescent diagnosed with familial hemiplegic migraine type 2 (FHM2), an autosomal dominant inheritance disorder caused by ATP1A2 mutation. We report the patient who presented with headache, aphasia, and left-sided weakness. Cerebrovascular disease and var...
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| Principais autores: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Frontiers Media S.A.
2024-02-01
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| Series: | Frontiers in Neurology |
| Assuntos: | |
| Acceso en liña: | https://www.frontiersin.org/articles/10.3389/fneur.2024.1339642/full |
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