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Published on: May 6, 2018
Late-onset nephrotic syndrome in galloway-mowat syndrome: a case report
1Department of Pediatrics, King Hussein Medical Center, Amman, Jordan.
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.
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