Familial left ventricular noncompaction cardiomyopathy due to a novel mutation in the MYH 7 gene

Left Ventricular Non Compaction (LVNC) is considered a unique cardiomyopathy according to the American Heart Association guidelines. The genetic ethology of LVNC in children is not completely understood although upto 41% of LVNC are thought to be genetic. We report a family with LVNC due to a novel...

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Autores principales: Alawani, Sujata S, Paul, Abraham, Krishna, Mani Ram, Ahamed, Hisham
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9075559/
https://www.ncbi.nlm.nih.gov/pubmed/35527761
http://dx.doi.org/10.4103/apc.APC_92_20
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author Alawani, Sujata S
Paul, Abraham
Krishna, Mani Ram
Ahamed, Hisham
author_facet Alawani, Sujata S
Paul, Abraham
Krishna, Mani Ram
Ahamed, Hisham
author_sort Alawani, Sujata S
collection PubMed
description Left Ventricular Non Compaction (LVNC) is considered a unique cardiomyopathy according to the American Heart Association guidelines. The genetic ethology of LVNC in children is not completely understood although upto 41% of LVNC are thought to be genetic. We report a family with LVNC due to a novel mutation in the MYH 7 gene.
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spelling pubmed-90755592022-05-07 Familial left ventricular noncompaction cardiomyopathy due to a novel mutation in the MYH 7 gene Alawani, Sujata S Paul, Abraham Krishna, Mani Ram Ahamed, Hisham Ann Pediatr Cardiol Case Report Left Ventricular Non Compaction (LVNC) is considered a unique cardiomyopathy according to the American Heart Association guidelines. The genetic ethology of LVNC in children is not completely understood although upto 41% of LVNC are thought to be genetic. We report a family with LVNC due to a novel mutation in the MYH 7 gene. Wolters Kluwer - Medknow 2021 2022-03-25 /pmc/articles/PMC9075559/ /pubmed/35527761 http://dx.doi.org/10.4103/apc.APC_92_20 Text en Copyright: © 2022 Annals of Pediatric Cardiology https://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
Alawani, Sujata S
Paul, Abraham
Krishna, Mani Ram
Ahamed, Hisham
Familial left ventricular noncompaction cardiomyopathy due to a novel mutation in the MYH 7 gene
title Familial left ventricular noncompaction cardiomyopathy due to a novel mutation in the MYH 7 gene
title_full Familial left ventricular noncompaction cardiomyopathy due to a novel mutation in the MYH 7 gene
title_fullStr Familial left ventricular noncompaction cardiomyopathy due to a novel mutation in the MYH 7 gene
title_full_unstemmed Familial left ventricular noncompaction cardiomyopathy due to a novel mutation in the MYH 7 gene
title_short Familial left ventricular noncompaction cardiomyopathy due to a novel mutation in the MYH 7 gene
title_sort familial left ventricular noncompaction cardiomyopathy due to a novel mutation in the myh 7 gene
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9075559/
https://www.ncbi.nlm.nih.gov/pubmed/35527761
http://dx.doi.org/10.4103/apc.APC_92_20
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