A Fetus with Hypertrophic Cardiomyopathy, Restrictive, and Single-Ventricle Physiology, and a β-Myosin Heavy Chain Mutation

Robert B. Hinton, Erik C. Michelfelder, Bradley S. Marino, Kevin E. Bove, Stephanie Ware

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

Cardiomyopathy is a significant clinical problem associated with sudden death. A molecular taxonomy is emerging that is refining the clinical classification system. We describe a patient with a pathogenic familial β-myosin heavy chain mutation who was prenatally diagnosed with left ventricular hypoplasia and restrictive diastolic physiology.

Original languageEnglish (US)
Pages (from-to)164-166
Number of pages3
JournalJournal of Pediatrics
Volume157
Issue number1
DOIs
StatePublished - Jul 2010
Externally publishedYes

Fingerprint

Myosin Heavy Chains
Hypertrophic Cardiomyopathy
Fetus
Mutation
Sudden Death
Cardiomyopathies

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

Cite this

A Fetus with Hypertrophic Cardiomyopathy, Restrictive, and Single-Ventricle Physiology, and a β-Myosin Heavy Chain Mutation. / Hinton, Robert B.; Michelfelder, Erik C.; Marino, Bradley S.; Bove, Kevin E.; Ware, Stephanie.

In: Journal of Pediatrics, Vol. 157, No. 1, 07.2010, p. 164-166.

Research output: Contribution to journalArticle

Hinton, Robert B. ; Michelfelder, Erik C. ; Marino, Bradley S. ; Bove, Kevin E. ; Ware, Stephanie. / A Fetus with Hypertrophic Cardiomyopathy, Restrictive, and Single-Ventricle Physiology, and a β-Myosin Heavy Chain Mutation. In: Journal of Pediatrics. 2010 ; Vol. 157, No. 1. pp. 164-166.
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