Juvenile Huntington’s disease masquerading as progressive myoclonus epilepsy

Juvenile Huntington’s disease (JHD) has an onset before 20 years of age, and is characterized by behavioural issues, epilepsy, rigidity, bradykinesia and dystonia. It contributes to 0.5–5% of all Huntington disease (HD) cases. JHD demonstrates a more rapid progression and is characterised by dystoni...

Descripción completa

Detalles Bibliográficos
Autores principales: Thakor, Bina, Jagtap, Sujit A., Joshi, Aniruddha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8327331/
https://www.ncbi.nlm.nih.gov/pubmed/34377971
http://dx.doi.org/10.1016/j.ebr.2021.100470

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8327331/
https://www.ncbi.nlm.nih.gov/pubmed/34377971
http://dx.doi.org/10.1016/j.ebr.2021.100470

Ejemplares similares