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Pediatric Cardiology
Published in: Pediatric Cardiology 8/2013

01-12-2013 | Case Report

Noonan Syndrome and Different Morphologic Expressions of Hypertrophic Cardiomyopathy

Authors: Efrén Martínez-Quintana, Fayna Rodríguez-González, Paula Junquera-Rionda

Published in: Pediatric Cardiology | Issue 8/2013

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Abstract

Hypertrophic cardiomyopathy is the disease with the largest heterogeneity in clinical cardiology. An underrecognized and incompletely described subgroup within this spectrum comprises patients with ventricular diverticulum, coronary myocardial bridging, and left ventricular crypts and crevices. This report presents the case of a Noonan syndrome patient with these four hypertrophic cardiomyopathy characteristics.
Literature
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Digilio MC, Marino B, Picchio F, Prandstraller D, Toscano A, Giannotti A et al (1998) Noonan syndrome and aortic coarctation. Am J Med Genet 80:160–162CrossRefPubMed
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Leye M, Calcagni G, Brunelle F, Bonnet D, Sidi D, Ou P (2009) Coronary myocardial bridging in Noonan syndrome: definitive diagnosis with high-resolution CT. Br J Radiol 82:e8–e10CrossRefPubMed
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Makkuni P, Kotler MN, Figueredo VM (2010) Diverticular and aneurysmal structures of the left ventricle in adults: report of a case within the context of a literature review. Tex Heart Inst J 37:699–705PubMedCentralPubMed
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Maron BJ, Lindberg J, Lesser JR (2010) Ventricular septal crypt in hypertrophic cardiomyopathy. Eur Heart J 31:1923CrossRefPubMed
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Metadata
Title
Noonan Syndrome and Different Morphologic Expressions of Hypertrophic Cardiomyopathy
Authors
Efrén Martínez-Quintana
Fayna Rodríguez-González
Paula Junquera-Rionda
Publication date
01-12-2013
Publisher
Springer US
Published in
Pediatric Cardiology / Issue 8/2013
Print ISSN: 0172-0643
Electronic ISSN: 1432-1971
DOI
https://doi.org/10.1007/s00246-012-0424-3

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