Combined cardiac anomalies in Noonan syndrome: A case report

INTRODUCTION: Noonan syndrome is the second most common syndromic cause of congenital heart disease. Most patients have an autosomal dominant inheritance, but some cases may be sporadic. Pulmonary stenosis is the most common cardiac manifestation in Noonan syndrome, associated with the atrial septal...

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Detalles Bibliográficos
Autores principales: H.S., Natraj Setty, S., Shankar, Patil, Rahul, Jadhav, Santosh, M.C., Yeriswamy, Reddy, Babu, Kharge, Jayashree, Raghu, T.R., Shankar, Sandeep, Raj, Sathwik, N., Chethan, M., Nithin, Manjunath, C.N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7276397/
https://www.ncbi.nlm.nih.gov/pubmed/32506025
http://dx.doi.org/10.1016/j.ijscr.2020.05.048

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7276397/
https://www.ncbi.nlm.nih.gov/pubmed/32506025
http://dx.doi.org/10.1016/j.ijscr.2020.05.048

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