Case series of autosomal recessive hereditary spastic paraparesis with novel mutation in SPG 7 gene

Autosomal recessive hereditary spastic paraparesis is rare.We present 4 patients with slowly progressive predominantly lower limb spasticity and ataxia. Only one patient had family history of ataxia but without any underlying diagnosis. All of them proved negative for the mutation of Spinocerebelalr...

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Detalles Bibliográficos
Autores principales: Bhattacharjee, Shakya, Beauchamp, Nicholas, Murray, Brian E., Lynch, Timothy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Riyadh : Armed Forces Hospital 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5946381/
https://www.ncbi.nlm.nih.gov/pubmed/29057857
http://dx.doi.org/10.17712/nsj.2017.4.20170253

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5946381/
https://www.ncbi.nlm.nih.gov/pubmed/29057857
http://dx.doi.org/10.17712/nsj.2017.4.20170253

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