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Childhood-onset (Juvenile) Huntington's disease: A rare case report

Huntington's disease (HD) is a rare dominantly inherited neurodegenerative disorder characterized clinically by a combination of abnormal involuntary (choreic) movements, neuropsychiatric manifestations, and dementia. It is caused by an unstable CAG repeat expansion in the gene IT15 which encod...

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Detalles Bibliográficos
Autores principales:	Patra, Kailash Chandra, Shirolkar, Mukund Sudhir
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2015
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4611904/ https://www.ncbi.nlm.nih.gov/pubmed/26557176 http://dx.doi.org/10.4103/1817-1745.165709

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