Congenital arch vessel anomalies in CHARGE syndrome: A frequent feature with risk for co-morbidity()()

BACKGROUND: CHARGE syndrome is a complex multiple congenital malformation disorder with variable expression that is caused by mutations in the CHD7 gene. Variable heart defects occur in 74% of patients with a CHD7 mutation, with an overrepresentation of atrioventricular septal defects and conotrunca...

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Detalles Bibliográficos
Autores principales: Corsten-Janssen, Nicole, van Ravenswaaij-Arts, Conny M.A., Kapusta, Livia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5454153/
https://www.ncbi.nlm.nih.gov/pubmed/28616537
http://dx.doi.org/10.1016/j.ijcha.2016.05.015

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5454153/
https://www.ncbi.nlm.nih.gov/pubmed/28616537
http://dx.doi.org/10.1016/j.ijcha.2016.05.015

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