Cargando…
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...
Autores principales: | Alawani, Sujata S, Paul, Abraham, Krishna, Mani Ram, Ahamed, Hisham |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2021
|
Materias: | |
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 |
Ejemplares similares
-
A Splice Variant of the MYH7 Gene Is Causative in a Family with Isolated Left Ventricular Noncompaction Cardiomyopathy
por: Myasnikov, Roman P., et al.
Publicado: (2022) -
Left ventricular noncompaction cardiomyopathy
por: Hawatmeh, Amer, et al.
Publicado: (2017) -
Pregnancy in Familial Left Ventricular Noncompaction-Associated Cardiomyopathy
por: Crousillat, Daniela R., et al.
Publicado: (2020) -
A Novel Missense Variant in Actin Binding Domain of MYH7 Is Associated With Left Ventricular Noncompaction
por: Hesaraki, Mahdi, et al.
Publicado: (2022) -
Nexilin mutations are associated with left ventricular noncompaction cardiomyopathy
por: Pardun, E, et al.
Publicado: (2015)