Membranous nephropathy in Schimke immuno-osseous dysplasia


Ozdemir N., Alpay H., Bereket A., Bereket G., Biyikli N., Aydogan M. , et al.

PEDIATRIC NEPHROLOGY, cilt.21, ss.870-872, 2006 (SCI İndekslerine Giren Dergi) identifier identifier identifier

  • Cilt numarası: 21 Konu: 6
  • Basım Tarihi: 2006
  • Doi Numarası: 10.1007/s00467-006-0082-x
  • Dergi Adı: PEDIATRIC NEPHROLOGY
  • Sayfa Sayısı: ss.870-872

Özet

Schimke 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.