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Title: Galloway-mowat syndrome - unusual form of nephrotic syndrome in adolescent. Author: Naidu GD, Deepthi P, RajaKarthik K, Sriram S, Swarnalatha G, Gangadhar T. Journal: Saudi J Kidney Dis Transpl; 2017; 28(5):1188-1191. PubMed ID: 28937085. Abstract: Galloway-Mowat syndrome (GMS), also acknowledged as Microcephaly-Hiatal hernia nephrotic syndrome, is an uncommon genetic disorder inherited as an autosomal recessive trait usually seen before two years of life. It is an exceptional multisystem genetic disorder with a collection of skeletal, neurological, facial, gastrointestinal, growth, and renal abnormalities. This case report describes GMS in a girl, suffering from developmental delay, stunted growth, and various dysmorphic features, in whom nephrotic syndrome became apparent at adolescent age.[Abstract] [Full Text] [Related] [New Search]