Arslan, D.Cimen, D.Guvenc, O.Sert, A.Oktay, A.Oran, B.2020-03-262020-03-2620141015-8146https://hdl.handle.net/20.500.12395/30525A case of Seckel syndrome with tricuspid atresia: Seckel syndrome is an autosomal recessive disease presenting with marked growth retardation, microcephalic dwarfism, some facial and skeletal abnormalities. Tricuspid atresia is a rare and life threatening cyanotic congenital heart diseases, with an incidence of 1% to 3%. It is feature of the anatomically normally related great arteries with a large ventricular septum defect and stenosis of right ventricular outflow tract. Tricuspid atresia has never been reported in patients with Seckel syndrome. Here we report a 15-day-old girl baby diagnosed as having Seckel syndrome with tricuspid atresia.eninfo:eu-repo/semantics/closedAccessSeckel syndromeTricuspid atresiaChildArticle25217117525059015N/AWOS:000338752600006Q4