Case Report: Restrictive cardiomyopathy due to a rare mutation in troponin I gene (TNNI3) in a patient

Case Report: Restrictive cardiomyopathy due to a rare mutation in troponin I gene (TNNI3) in a patient

BackgroundRestrictive cardiomyopathy (RCM) is a rare cardiomyopathy often characterized by normal or reduced ventricular chamber volume and bi-atrial enlargement, caused mainly by mutations in the myonodal gene. It has a low incidence, non-specific clinical manifestations, rapid progression, and lac...

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Bibliographic Details
Main Authors: Lili Deng, Liming Luo, Min Zhang, Cheng Guo, Kai Liu
Format: Article
Language:English
Published: Frontiers Media S.A. 2024-11-01
Series:Frontiers in Cardiovascular Medicine
Subjects:
TNNI3gene
mutation
restrictive cardiomyopathy
children
case
Online Access:https://www.frontiersin.org/articles/10.3389/fcvm.2024.1456542/full
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