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Seckel syndrome with Morgagni hernia
Authors:Onder Asan  Cogulu Ozgur  Ekmekci Aslihan  Pariltay Erhan  Kirbiyik Ozgur  Ozkinay Ferda
Affiliation:Department of Pediatrics, Faculty of Medicine, Ege University, Izmir, Turkey.
Abstract:Seckel syndrome is an autosomal recessive disease presenting with microcephalic dwarfism, mental retardation and facial and skeletal abnormalities. Morgagni hernia is quite rare, constituting 1-6% of all diaphragmatic hernias. It is asymptomatic, especially in childhood. Morgagni hernia has never been reported in patients with Seckel Syndrome. Here we report a 3-year-old boy diagnosed as having Seckel Syndrome with Morgagni hernia, which has to be considered during physical examination of patients.
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