Biventricular Noncompaction Cardiomyopathy Accompanied by Severe Pulmonary Valvular Stenosis and Patent Foramen Ovale

Myocardial non-compaction (NC) is a rare genetic cardiomyopathy commonly believed to develop an intrauterine arrest of endomyocardial morphogenesis. NC is characterized by markedly hypertrabeculations in left ventricle or both ventricles with deep intertrabecular recesses. NC is usually seen isolate...

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Autores principales: Karauzum, Kurtulus, Karauzum, Irem Yilmaz, Sahin, Tayfun, Kilic, Teoman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5989548/
https://www.ncbi.nlm.nih.gov/pubmed/29911014
http://dx.doi.org/10.4103/jcecho.jcecho_50_17
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author Karauzum, Kurtulus
Karauzum, Irem Yilmaz
Sahin, Tayfun
Kilic, Teoman
author_facet Karauzum, Kurtulus
Karauzum, Irem Yilmaz
Sahin, Tayfun
Kilic, Teoman
author_sort Karauzum, Kurtulus
collection PubMed
description Myocardial non-compaction (NC) is a rare genetic cardiomyopathy commonly believed to develop an intrauterine arrest of endomyocardial morphogenesis. NC is characterized by markedly hypertrabeculations in left ventricle or both ventricles with deep intertrabecular recesses. NC is usually seen isolated, but sometimes other congenital heart abnormalities may accompany to the myocardial NC. In this article we have presented an adult patient with biventricular myocardial NC cardiomyopathy accompanied by severe valvular pulmonary stenosis and patent foramen ovale.
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spelling pubmed-59895482018-06-15 Biventricular Noncompaction Cardiomyopathy Accompanied by Severe Pulmonary Valvular Stenosis and Patent Foramen Ovale Karauzum, Kurtulus Karauzum, Irem Yilmaz Sahin, Tayfun Kilic, Teoman J Cardiovasc Echogr Case Report Myocardial non-compaction (NC) is a rare genetic cardiomyopathy commonly believed to develop an intrauterine arrest of endomyocardial morphogenesis. NC is characterized by markedly hypertrabeculations in left ventricle or both ventricles with deep intertrabecular recesses. NC is usually seen isolated, but sometimes other congenital heart abnormalities may accompany to the myocardial NC. In this article we have presented an adult patient with biventricular myocardial NC cardiomyopathy accompanied by severe valvular pulmonary stenosis and patent foramen ovale. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC5989548/ /pubmed/29911014 http://dx.doi.org/10.4103/jcecho.jcecho_50_17 Text en Copyright: © 2018 Journal of Cardiovascular Echography http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Karauzum, Kurtulus
Karauzum, Irem Yilmaz
Sahin, Tayfun
Kilic, Teoman
Biventricular Noncompaction Cardiomyopathy Accompanied by Severe Pulmonary Valvular Stenosis and Patent Foramen Ovale
title Biventricular Noncompaction Cardiomyopathy Accompanied by Severe Pulmonary Valvular Stenosis and Patent Foramen Ovale
title_full Biventricular Noncompaction Cardiomyopathy Accompanied by Severe Pulmonary Valvular Stenosis and Patent Foramen Ovale
title_fullStr Biventricular Noncompaction Cardiomyopathy Accompanied by Severe Pulmonary Valvular Stenosis and Patent Foramen Ovale
title_full_unstemmed Biventricular Noncompaction Cardiomyopathy Accompanied by Severe Pulmonary Valvular Stenosis and Patent Foramen Ovale
title_short Biventricular Noncompaction Cardiomyopathy Accompanied by Severe Pulmonary Valvular Stenosis and Patent Foramen Ovale
title_sort biventricular noncompaction cardiomyopathy accompanied by severe pulmonary valvular stenosis and patent foramen ovale
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5989548/
https://www.ncbi.nlm.nih.gov/pubmed/29911014
http://dx.doi.org/10.4103/jcecho.jcecho_50_17
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