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Article

Merosin-deficient congenital muscular dystrophy and cortical dysplasia.

European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society - 1 Jan 1998

Brett F M, Costigan D, Farrell M A, Heaphy P, Thornton J, King M D

Abstract excerpt

Congenital muscular dystrophy (CMD) encompasses a heterogenous group of muscle disorders with autosomal recessive inheritance, characterized by muscular weakness and hypotonia at birth or within the first few months of life and developmental delay. Merosin-deficient CMD is a clinically distinct form which may be associated with significant abnormalities of the brain detectable by neuroimaging. We report two...

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Identifiers

PMID: 10724100
DOI: 10.1016/s1090-3798(98)80045-7

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

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