Late-onset nephrotic syndrome in galloway-mowat syndrome: a case report.

Abstract

Galloway-Mowat Syndrome (GMS) has a wide variety of clinical manifestations and histologic findings. All reported cases had developed nephrotic syndrome in the first two years of life. We report a case of 12 years old boy with microcephaly, mental retardation, and typical dysmorphic features of GMS with a late onset of minimal change nephritic syndrome which first manifested at seven years of age.

• Authors: I Hazza, A H Najada
• Journal: Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia (Saudi J Kidney Dis Transpl) Vol. 10 Issue 2 Pg. 171-4 ( 1999) ISSN: 1319-2442 [Print] Saudi Arabia
• PMID: 18212429 (Publication Type: Journal Article)