Atrial septal defect in a pediatric patient with Williams Syndrome: a rare presentation

Characterized by congenital heart defects (CHD) and elfin-like facies, Williams-Beuren syndrome (WS) is a multisystemic disorder that occurs approximately in 1 in 10 000 newborns [1]. WS is caused by a contiguous gene microdeletion of the Williams Beuren syndrome critical region (WBSCR) on chromosom...

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Detalles Bibliográficos
Autores principales: Grajeda, Javier, Mubarak, Amir N, Ardebol, Javier, Grajeda, Guillermo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9707007/
https://www.ncbi.nlm.nih.gov/pubmed/36458262
http://dx.doi.org/10.1093/jscr/rjac527

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9707007/
https://www.ncbi.nlm.nih.gov/pubmed/36458262
http://dx.doi.org/10.1093/jscr/rjac527

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