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Repair of double orifice mitral valve with an atrioventricular septal defect in a girl with Ellis–Van Creveld syndrome

Ellis–van Creveld syndrome is a rare autosomal recessive disorder caused by mutations in the EVC and EVC2 genes. The four principal manifestations are chondrodysplasia, polydactyly, ectodermal dysplasia, and congenital heart defects. We describe the case of a 7‐year‐old girl with Ellis–van Creveld S...

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Detalles Bibliográficos
Autores principales:	Al‐Dairy, Alwaleed, Srour, Samir, Chaker, Alaa, Alzahraa Alsyed Hasan, Fatimah
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2022
Materias:	Case Reports
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9117707/ https://www.ncbi.nlm.nih.gov/pubmed/35600041 http://dx.doi.org/10.1002/ccr3.5888

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