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Adult‐onset Niemann–Pick disease type C masquerading as spinocerebellar ataxia
BACKGROUND: Adult‐onset Nieman–Pick disease type C (NPC) is a rare progressive ataxia caused by lysosomal accumulation of unesterified cholesterol resulting in severe disability and death. The diagnosis of NPC can be challenging as clinical features overlap with other more common hereditary ataxias....
Autores principales: | Vo, Mary L., Levy, Tess, Lakhani, Shenela, Wang, Chengbing, Ross, M. Elizabeth |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9000929/ https://www.ncbi.nlm.nih.gov/pubmed/35192242 http://dx.doi.org/10.1002/mgg3.1906 |
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