Serial magnetic resonance imaging findings during severe attacks of familial hemiplegic migraine type 2: a case report

BACKGROUND: Hemiplegic migraines represent a heterogeneous disorder with various presentations. Hemiplegic migraines are classified as sporadic or familial based on the presence of family history, but both subtypes have an underlying genetic etiology. Mutations in the ATP1A2 gene are responsible for...

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Detalles Bibliográficos
Autores principales: Fear, David, Patel, Misha, Zand, Ramin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8059280/
https://www.ncbi.nlm.nih.gov/pubmed/33882852
http://dx.doi.org/10.1186/s12883-021-02201-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8059280/
https://www.ncbi.nlm.nih.gov/pubmed/33882852
http://dx.doi.org/10.1186/s12883-021-02201-z

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