Galloway-mowat syndrome - unusual form of nephrotic syndrome in adolescent

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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.

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Naidu, G. D., Deepthi, P., RajaKarthik, K., Sriram, S., Swarnalatha, G., & Gangadhar, T. (2017). Galloway-mowat syndrome - unusual form of nephrotic syndrome in adolescent. Saudi Journal of Kidney Diseases and Transplantation : An Official Publication of the Saudi Center for Organ Transplantation, Saudi Arabia, 28(5), 1188–1191. https://doi.org/10.4103/1319-2442.215154

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