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Article

Hypertrophic cardiomyopathy: a new mutation illustrates the need for family-centered care.

Pediatric cardiology - 1 Dec 2014

Lee Daniel D, Veith Regan L, Dimmock David P, Samyn Margaret M

Abstract excerpt

This is a case series of a family positive for a previously undescribed mutation in the myofilament gene MYH7, causing hypertrophic cardiomyopathy (HCM), a potentially lethal cardiac disease with strong hereditability. The family's significant disease became strikingly apparent with the unanticipated diagnosis of their newborn infant shortly after her birth. This led to the discovery of the MYH7 mutation in the...

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Source

Identifiers

PMID: 25182012
DOI: 10.1007/s00246-014-1002-7

Genes

MYH7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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