Erschienen in:
01.05.2013 | e-Herz: Case study
Two different cardiomyopathies in a single patient
Hypertrophic cardiomyopathy and left ventricular noncompaction
verfasst von:
M. Sunbul, Assoc. Prof. B. Ozben, MD, B. Mutlu
Erschienen in:
Herz
|
Ausgabe 3/2013
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Abstract
Hypertrophic cardiomyopathy is a complex and relatively common genetic disorder characterized by left ventricular (LV) hypertrophy, usually associated with a nondilated and hyperdynamic chamber with heterogeneous phenotypic expression and clinical course. On the other hand, LV noncompaction is an uncommon cardiomyopathy characterized by the persistence of fetal myocardium with a pattern of prominent trabecular meshwork and deep intertrabecular recesses, systolic dysfunction, and LV dilatation. We report a 29-year-old man with these two different inherent conditions. Our case raises the possibility of a genetic mutation common to these two clinical entities or different gene mutations existing in the same individual.