Psychiatric morbidity and poor follow-up underlie suboptimal functional and survival outcomes in Huntington’s disease

BACKGROUND: Huntington’s disease (HD), an inherited, often late-onset, neurodegenerative disorder, is considered to be a rare, orphan disease. Research into its genetic correlates and services for those affected are inadequate in most low-middle income countries, including India. The apparent ‘incur...

Descripción completa

Detalles Bibliográficos
Autores principales: Ratna, Nikhil, Kamble, Nitish L., Venkatesh, Sowmya D., Purushottam, Meera, Pal, Pramod K., Jain, Sanjeev
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7068943/
https://www.ncbi.nlm.nih.gov/pubmed/32164608
http://dx.doi.org/10.1186/s12883-020-01671-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7068943/
https://www.ncbi.nlm.nih.gov/pubmed/32164608
http://dx.doi.org/10.1186/s12883-020-01671-x

Ejemplares similares