Case report and literature review of Huntington disease with intermediate CAG expansion

BACKGROUND: Huntington disease (HD) is a genetically inherited neurodegenerative disorder that classically involves a trinucleotide CAG repeat expansion on chromosome 4, with 36 repeats or greater being disease identifying. It generally presents between the age of 30 and 40 years old and is characte...

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Detalles Bibliográficos
Autores principales: Jevtic, Stefan D, Provias, John P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
Materias:
Short Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7871728/
https://www.ncbi.nlm.nih.gov/pubmed/33681777
http://dx.doi.org/10.1136/bmjno-2019-000027

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7871728/
https://www.ncbi.nlm.nih.gov/pubmed/33681777
http://dx.doi.org/10.1136/bmjno-2019-000027

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