Epilepsie révélant une chorée-acanthocytose: à propos d’un cas

Chorea-acanthocytosis (ChAc) is an extremely rare autosomal recessive disorder caused by mutations in the VSP13A gene on chromosome 9q21. It is characterized by neurological symptoms, psychiatric manifestations and multisystem involvement resulting in myopathy, axonal neuropathy and presence of spic...

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Detalles Bibliográficos
Autores principales: Doghmi, Nawfal, Elkoundi, Abdelghafour, Meskine, Amine, Benakrout, Aziz, Baite, Abdelouahed, Haimeur, Cherqui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5072886/
https://www.ncbi.nlm.nih.gov/pubmed/27795769
http://dx.doi.org/10.11604/pamj.2016.24.172.9686

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5072886/
https://www.ncbi.nlm.nih.gov/pubmed/27795769
http://dx.doi.org/10.11604/pamj.2016.24.172.9686

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