Spinocerebellar ataxia 2 in a family with different phenotypes: Two case reports

RATIONALE: Spinocerebellar ataxia 2 (SCA2) is a genetic disease, mainly characterized by ataxia. A number of other neurological symptoms also have been described, such as Parkinsonism, cognitive dysfunction, autonomic dysfunction, even the signs of motor neuron disease and so on. Mostly, In the same...

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Detalles Bibliográficos
Autores principales: Li, Yuanyuan, Chang, Ying, Liu, Xiufeng, Li, Yanyan, Yan, Yayun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
3500
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6867747/
https://www.ncbi.nlm.nih.gov/pubmed/31725623
http://dx.doi.org/10.1097/MD.0000000000017834

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6867747/
https://www.ncbi.nlm.nih.gov/pubmed/31725623
http://dx.doi.org/10.1097/MD.0000000000017834

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