Seckel syndrome with Morgagni hernia |
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Authors: | Onder Asan Cogulu Ozgur Ekmekci Aslihan Pariltay Erhan Kirbiyik Ozgur Ozkinay Ferda |
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Affiliation: | Department of Pediatrics, Faculty of Medicine, Ege University, Izmir, Turkey. |
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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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