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.
CITATION STYLE
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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