Article

Utilization of CoRDS Registry to Monitor Quality of Life in Patients with VCP Multisystem Proteinopathy

2024-08-20

Abstract excerpt

<h4>Background</h4> VCP disease, also known as multisystem proteinopathy (MSP1), 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 Myopathy (IBM), Paget’s disease of bone (PDB), Frontotemporal Dementia (IBMPFD), and Amyotrophic Lateral Scle...

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Literature Corpus work: 7c33b0ac-1533-594a-a832-0878b1915926
DOI: 10.1101/2024.08.18.24311141

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