Medullary nephrocalcinosis in Schimke immuno‐osseous dysplasia

Schimke immuno‐osseous dysplasia (SIOD) is a rare hereditary disease characterized by skeletal dysplasia, immune deficiency and progressive renal disease. Kidney involvement mainly determines the prognosis. The most common renal pathology is focal segmental glomerulosclerosis (FSGS). Medullary nephr...

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Veröffentlicht in:Pediatrics international 2015-04, Vol.57 (2), p.310-313
Hauptverfasser: Yavuz, Sevgi, Bayazıt, Aysun Karabay, Anarat, Ali, Gonlusen, Gulfiliz, Alsancak, Perihan
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Sprache:eng
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Zusammenfassung:Schimke immuno‐osseous dysplasia (SIOD) is a rare hereditary disease characterized by skeletal dysplasia, immune deficiency and progressive renal disease. Kidney involvement mainly determines the prognosis. The most common renal pathology is focal segmental glomerulosclerosis (FSGS). Medullary nephrocalcinosis refers to the diffuse deposition of calcium salts in renal medulla and has not previously been identified in SIOD. Here we report the first case of a pediatric patient having typical features of SIOD with medullary nephrocalcinosis.
ISSN:1328-8067
1442-200X
DOI:10.1111/ped.12455