Early Diagnosis of Abnormal Left Ventricular Systolic Functions of Rare Pathogenic Titin Mutation Gene Carriers in FHCM by Three-Dimensional Speckle Tracking Echocardiography Combined with Gene Detection

OBJECTIVE: This study aimed to explore the early diagnosis of abnormal left ventricular systolic function of rare pathogenic titin (TTN) mutation gene carriers in familial hypertrophic cardiomyopathy (FHCM) by three-dimensional speckle tracking echocardiography (3D-STE) combined with gene detection....

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Detalles Bibliográficos
Autores principales: Luo, Xiang-hong, Zhu, Rui, Chen, Qian, Shi, Pei-hong, Na, Li-sha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9578807/
https://www.ncbi.nlm.nih.gov/pubmed/36304977
http://dx.doi.org/10.1155/2022/3415545

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9578807/
https://www.ncbi.nlm.nih.gov/pubmed/36304977
http://dx.doi.org/10.1155/2022/3415545

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