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Article

Congenital muscular dystrophy. Part I: a review of phenotypical and diagnostic aspects.

Arquivos de neuro-psiquiatria - 1 Mar 2009

Reed Umbertina Conti

Abstract excerpt

The congenital muscular dystrophies (CMDs) are a group of genetically and clinically heterogeneous hereditary myopathies with preferentially autosomal recessive inheritance, that are characterized by congenital hypotonia, delayed motor development and early onset of progressive muscle weakness associated with dystrophic pattern on muscle biopsy. The clinical course is broadly variable and can comprise the...

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PMID: 19330236
DOI: 10.1590/s0004-282x2009000100038

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

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