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Article

Duchenne muscular dystrophy and idiopathic hyperCKemia segregating in a family.

American journal of medical genetics - 11 Sept 1995

Frydman M, Straussberg R, Shomrat R, Goebel H, Legum C, Shiloh Y

Abstract excerpt

A 7-month-old boy with gross motor delay and failure to thrive presented with rhabdomyolysis following an acute asthmatic episode. During hospitalization an electrocardiographic conversion to a Wolff-Parkinson-White type 1 (WPW) pattern took place. Duchenne muscular dystrophy (DMD) was suspected...

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Source

Identifiers

PMID: 8533818
DOI: 10.1002/ajmg.1320580302

Genes

DMD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-8533818-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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Duchenne muscular dystrophy and idiopathic hyperCKemia segregating in a family.PMID 8533818Read ↗

Duchenne muscular dystrophy and idiopathic hyperCKemia in the same family.Semantic proximity Read ↗

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A novel DMD splicing mutation found in a family responsible for X-linked dilated cardiomyopathy with hyper-CKemia.Semantic proximity Read ↗

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