Clinical and Genetic Screening for Hypertrophic Cardiomyopathy in Paediatric Relatives: Changing Paradigms in Clinical Practice

Hypertrophic cardiomyopathy (HCM) is an important cause of morbidity and mortality in children. While the aetiology is heterogeneous, most cases are caused by variants in the genes encoding components of the cardiac sarcomere, which are inherited as an autosomal dominant trait. In recent years, ther...

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Detalles Bibliográficos
Autores principales: Lawley, Claire M., Kaski, Juan Pablo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10146293/
https://www.ncbi.nlm.nih.gov/pubmed/37109125
http://dx.doi.org/10.3390/jcm12082788

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10146293/
https://www.ncbi.nlm.nih.gov/pubmed/37109125
http://dx.doi.org/10.3390/jcm12082788

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