BEREKET, ABDULLAHALPAY, HARİKA2022-03-122022-03-1220060931-041Xhttps://hdl.handle.net/11424/228304Schimke immuno-osseous dysplasia is a rare autosomal recessive multi-system disorder, with clinical features of growth retardation, spondylo-epiphyseal dysplasia, nephrotic syndrome and immunodeficiency beginning in childhood. Here, we report a new case, in a 10-year-old boy with characteristic symptoms of Schimke immuno-osseous dysplasia. The patient presented with short stature and, later, developed nephrotic syndrome and peritonitis. In addition, he had perinuclear anti-neutrophilic cytoplasmic antibody (p-ANCA)-positive arthritis. Renal pathology of the patients with this disease usually show focal segmental glomerulonephritis, whereas our patient had membranous nephropathy, which has not previously been reported.enginfo:eu-repo/semantics/closedAccessSchimke immuno-osseous dysplasiamembranous nephropathyspondylo-epiphyseal dysplasianephrotic syndromegrowth failureNEPHROTIC SYNDROMESPONDYLOEPIPHYSEAL DYSPLASIADISEASEarticleWOS:00023756330002310.1007/s00467-006-0082-x165702011432-198X