Utilization of CoRDS registry to monitor quality of life in patients with VCP multisystem proteinopathy

Abstract Background VCP disease, also known as multisystem proteinopathy, is a rare, autosomal dominant, adult-onset, neuromuscular disease that is caused by variants in the valosin-containing protein (VCP) gene. VCP disease may exhibit one or more of the following primary features: inclusion body m...

Descripció completa

Dades bibliogràfiques

Autors principals:	Eiman Abdoalsadig, Merwa Hamid, Allison Peck, Leepakshi Johar, Virginia Kimonis
Format:	Artigo
Idioma:	Inglês
Publicat:	BMC 2025-04-01
Col·lecció:	Orphanet Journal of Rare Diseases
Matèries:	VCP Inclusion body myopathy Paget’s disease of bone Frontotemporal dementia (IBMPFD) Amyotrophic lateral sclerosis (ALS) Multisystem proteinopathy
Accés en línia:	https://doi.org/10.1186/s13023-025-03567-w
Etiquetes:	Afegir etiqueta Sense etiquetes, Sigues el primer a etiquetar aquest registre!