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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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| Publicado no: | Pan Afr Med J |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The African Field Epidemiology Network
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5072886/ https://ncbi.nlm.nih.gov/pubmed/27795769 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11604/pamj.2016.24.172.9686 |
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