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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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| Yayımlandı: | J Pediatr Neurosci |
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| Asıl Yazarlar: | , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Medknow Publications & Media Pvt Ltd
2015
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4611904/ https://ncbi.nlm.nih.gov/pubmed/26557176 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/1817-1745.165709 |
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