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Congenital muscular dystrophies: What is new?

Neuromuscular disorders : NMD - 1 Oct 2021

Zambon Alberto A, Muntoni Francesco

Abstract excerpt

Congenital muscular dystrophies (CMDs) are a group of inherited conditions defined by muscle weakness occurring before the acquisition of ambulation, delayed motor milestones, and characterised by muscle dystrophic pathology. A large number of genes - at least 35- are responsible for CMD phenotypes, and it is therefore not surprising that CMDs comprise a wide spectrum of phenotypes, with variable involvement of...

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PMID: 34470717
DOI: 10.1016/j.nmd.2021.07.009

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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