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...

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Detalles Bibliográficos
Autores principales: Lesinskienė, Sigita, Rojaka, Darja, Praninskienė, Rūta, Morkūnienė, Aušra, Matulevičienė, Aušra, Utkus, Algirdas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7528384/
https://www.ncbi.nlm.nih.gov/pubmed/32998776
http://dx.doi.org/10.1186/s13256-020-02494-7