Spinocerebellar ataxia type-7: Report of a family in Northwest Nigeria

Spinocerebellar ataxia type-7 (SCA7) is a cytosine-adenine-guanine (CAG) repeat polyglutamine disorder characterized by progressive degeneration of the cerebellum, brainstem, spinal cord, and retina. Clinical features include progressive ataxia, visual loss, pyramidal weakness, sensory impairment, a...

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Detalles Bibliográficos
Autores principales: Alkali, Nura Hamidu, Bwala, Sunday A., Alimi, Saeed A., Oyakhire, Shyngle I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402823/
https://www.ncbi.nlm.nih.gov/pubmed/27044733
http://dx.doi.org/10.4103/1596-3519.176205

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402823/
https://www.ncbi.nlm.nih.gov/pubmed/27044733
http://dx.doi.org/10.4103/1596-3519.176205

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