Case Report: Whole Exome Sequencing Identifies Compound Heterozygous Variants in TSFM Gene Causing Juvenile Hypertrophic Cardiomyopathy

We report a case of hypertrophic cardiomyopathy and lactic acidosis in a 3-year-old female. Cardiac and skeletal muscles biopsies exhibited mitochondrial hyperplasia with decreased complex IV activity. Whole exome sequencing identified compound heterozygous variants, p.Arg333Trp and p.Val119Leu, in...

Descripción completa

Detalles Bibliográficos
Autores principales: Yang, Jamie O., Shaybekyan, Hapet, Zhao, Yan, Kang, Xuedong, Fishbein, Gregory A., Khanlou, Negar, Alejos, Juan C., Halnon, Nancy, Satou, Gary, Biniwale, Reshma, Lee, Hane, Van Arsdell, Glen, Nelson, Stanley F., Touma, Marlin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Cardiovascular Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8770926/
https://www.ncbi.nlm.nih.gov/pubmed/35071363
http://dx.doi.org/10.3389/fcvm.2021.798985

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8770926/
https://www.ncbi.nlm.nih.gov/pubmed/35071363
http://dx.doi.org/10.3389/fcvm.2021.798985

Ejemplares similares