Cardiovascular Abnormalities and Gene Mutations in Children With Noonan Syndrome

Background: Common cardiac abnormalities in Noonan syndrome (NS) include congenital heart diseases (CHD), pulmonary valve stenosis and hypertrophic cardiomyopathy (HCM). Molecular diagnoses are enabling earlier and more precise diagnosis of patients who have a subtle or atypical presentation. The ai...

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Detalles Bibliográficos
Autores principales: Sun, Ling, Xie, Yu-mei, Wang, Shu-shui, Zhang, Zhi-wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9234298/
https://www.ncbi.nlm.nih.gov/pubmed/35770001
http://dx.doi.org/10.3389/fgene.2022.915129

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9234298/
https://www.ncbi.nlm.nih.gov/pubmed/35770001
http://dx.doi.org/10.3389/fgene.2022.915129

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