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

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 hypop...

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Autors principals: Hinton, Robert B., Michelfelder, Erik C., Marino, Bradley S., Bove, Kevin E., Ware, Stephanie M.
Format: Artigo
Idioma:Inglês
Publicat: 2010
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2886151/
https://ncbi.nlm.nih.gov/pubmed/20394946
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jpeds.2010.02.044
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