Co-occurring Duchenne muscular dystrophy and hypertrophic cardiomyopathy in an adult with atypical cardiac phenotype

Animesh Tandon; Michael D. Taylor; Linda H. Cripe

doi:10.1017/S1047951114000067

Co-occurring Duchenne muscular dystrophy and hypertrophic cardiomyopathy in an adult with atypical cardiac phenotype

Animesh Tandon, Michael D. Taylor, Linda H. Cripe

Research output: Contribution to journal › Article › peer-review

3 Scopus citations

Abstract

We present the case of a 29-year-old man with mutation-positive Duchenne muscular dystrophy and mutation-positive hypertrophic cardiomyopathy. His cardiac phenotype has characteristics of both disorders; he manifests sub-epicardial left ventricular free wall late gadolinium enhancement that is consistent with Duchenne cardiomyopathy, as well as asymmetric ventricular septal hypertrophy, hyperdynamic left ventricular systolic function, and septal mid-myocardial late gadolinium enhancement, which are characteristic of hypertrophic cardiomyopathy.

Original language	English (US)
Pages (from-to)	355-357
Number of pages	3
Journal	Cardiology in the Young
Volume	25
Issue number	2
DOIs	https://doi.org/10.1017/S1047951114000067
State	Published - Nov 6 2015

Keywords

Duchenne muscular dystrophy
cardiac magnetic resonance imaging
hypertrophic cardiomyopathy

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health
Cardiology and Cardiovascular Medicine

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10.1017/S1047951114000067

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title = "Co-occurring Duchenne muscular dystrophy and hypertrophic cardiomyopathy in an adult with atypical cardiac phenotype",

abstract = "We present the case of a 29-year-old man with mutation-positive Duchenne muscular dystrophy and mutation-positive hypertrophic cardiomyopathy. His cardiac phenotype has characteristics of both disorders; he manifests sub-epicardial left ventricular free wall late gadolinium enhancement that is consistent with Duchenne cardiomyopathy, as well as asymmetric ventricular septal hypertrophy, hyperdynamic left ventricular systolic function, and septal mid-myocardial late gadolinium enhancement, which are characteristic of hypertrophic cardiomyopathy.",

keywords = "Duchenne muscular dystrophy, cardiac magnetic resonance imaging, hypertrophic cardiomyopathy",

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AU - Tandon, Animesh

AU - Taylor, Michael D.

AU - Cripe, Linda H.

N1 - Publisher Copyright: © Cambridge University Press 2014.

PY - 2015/11/6

Y1 - 2015/11/6

N2 - We present the case of a 29-year-old man with mutation-positive Duchenne muscular dystrophy and mutation-positive hypertrophic cardiomyopathy. His cardiac phenotype has characteristics of both disorders; he manifests sub-epicardial left ventricular free wall late gadolinium enhancement that is consistent with Duchenne cardiomyopathy, as well as asymmetric ventricular septal hypertrophy, hyperdynamic left ventricular systolic function, and septal mid-myocardial late gadolinium enhancement, which are characteristic of hypertrophic cardiomyopathy.

AB - We present the case of a 29-year-old man with mutation-positive Duchenne muscular dystrophy and mutation-positive hypertrophic cardiomyopathy. His cardiac phenotype has characteristics of both disorders; he manifests sub-epicardial left ventricular free wall late gadolinium enhancement that is consistent with Duchenne cardiomyopathy, as well as asymmetric ventricular septal hypertrophy, hyperdynamic left ventricular systolic function, and septal mid-myocardial late gadolinium enhancement, which are characteristic of hypertrophic cardiomyopathy.

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KW - cardiac magnetic resonance imaging

KW - hypertrophic cardiomyopathy

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Co-occurring Duchenne muscular dystrophy and hypertrophic cardiomyopathy in an adult with atypical cardiac phenotype

Abstract

Keywords

ASJC Scopus subject areas

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