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Juvenile Huntington’s disease: two case reports and a review of the literature
BACKGROUND: Huntington’s disease is a rare, autosomal dominant neurodegenerative disease characterized by motor, cognitive, and psychiatric symptoms. Usually, the disease symptoms first appear around the age of 40, but in 5–10% of cases, they manifest before the age of 21. This is then referred to a...
Kaydedildi:
| Yayımlandı: | J Med Case Rep |
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| Asıl Yazarlar: | , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BioMed Central
2020
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7528384/ https://ncbi.nlm.nih.gov/pubmed/32998776 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13256-020-02494-7 |
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