Cargando…
A Family with Myh7 Mutation and Different Forms of Cardiomyopathies
Background: Hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM) are common heart muscle disorders that are caused by pathogenic variants in sarcomere protein genes. In this study, we describe a variant in the MHY7 gene, segregating in a family having three different phenotypes of card...
Autores principales: | Catrina, Bianca Iulia, Batar, Florina, Baltat, Georgiana, Bitea, Cornel Ioan, Puia, Andreea, Stoia, Oana, Fleacă, Sorin Radu, Teodoru, Minodora |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10377388/ https://www.ncbi.nlm.nih.gov/pubmed/37509704 http://dx.doi.org/10.3390/biomedicines11072065 |
Ejemplares similares
-
Interactions between Metabolic Syndrome, MASLD, and Arterial Stiffening: A Single-Center Cross-Sectional Study
por: Solomon, Adelaida, et al.
Publicado: (2023) -
The contribution of mutations in MYH7 to the onset of cardiomyopathy
por: Bollen, I. A. E., et al.
Publicado: (2017) -
A rare case of familial restrictive cardiomyopathy, with mutations in MYH7 and ABCC9 genes
por: Neagoe, Oana, et al.
Publicado: (2019) -
A Rare Case of Polysplenia Syndrome Associated with Severe Cardiac Malformations and Congenital Alveolar Dysplasia in a One-Month-Old Infant: A Complete Macroscopic and Histopathologic Study
por: Mohor, Cosmin Ioan, et al.
Publicado: (2022) -
Genetic variations of β-MYH7 in hypertrophic cardiomyopathy and dilated cardiomyopathy
por: Tanjore, Reena, et al.
Publicado: (2010)