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 M. Ware

Research output: Contribution to journalArticle

3 Scopus citations


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
Issue number1
StatePublished - Jul 1 2010


ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

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