Saudi Journal of Kidney Diseases and Transplantation (Jan 2017)

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

  • G Diwakar Naidu,
  • Pathapati Deepthi,
  • K RajaKarthik,
  • S Sriram,
  • G Swarnalatha,
  • T Gangadhar

DOI
https://doi.org/10.4103/1319-2442.215154
Journal volume & issue
Vol. 28, no. 5
pp. 1188 – 1191

Abstract

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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.