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Coffin-Siris syndrome with the rarest constellation of congenital cardiac defects: A case report with review of literature

We report a case of type-A Coffin-Siris syndrome (CSS) with a unique constellation of congenital heart defects. A 17-year-old Indian boy was referred to our hospital for central cyanosis with features of right heart failure. The cardiac abnormalities included biventricular outflow tract obstruction,...

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Detalles Bibliográficos
Autores principales: Nemani, Lalita, Barik, Ramachandra, Patnaik, Amar Narayana, Mishra, Ramesh C, Rao, Amaresh M, Kapur, Pragati
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4189243/
https://www.ncbi.nlm.nih.gov/pubmed/25298701
http://dx.doi.org/10.4103/0974-2069.140859
Descripción
Sumario:We report a case of type-A Coffin-Siris syndrome (CSS) with a unique constellation of congenital heart defects. A 17-year-old Indian boy was referred to our hospital for central cyanosis with features of right heart failure. The cardiac abnormalities included biventricular outflow tract obstruction, small atrial septal defect (ASD), subaortic ventricular septal defect, drainage of left superior venacava to left atrial appendage, and aortic arch anomaly. Patient underwent successful right ventricular infundibular resection, subaortic membrane resection, closure of atrial and ventricular septal defect, rerouting left superior vena cava to left pulmonary artery and aortic valve replacement.