| Literature DB >> 26354575 |
Ashraf Bakr, Riham Eid1, Amr Sarhan, Ayman Hammad, Ahmed Mahmoud El-Refaey, Atef El-Mougy, Mohammed Magdy Zedan, Fatma ElHusseini.
Abstract
Schimke immune-osseous dysplasia (SIOD) is a rare autosomal recessive disorder characterized by spondylo-epiphyseal dysplasia (SED), progressive renal insufficiency beginning as steroid-resistant nephrotic syndrome (SRNS) and defective cellular immunity. This article reports a case from Egypt with a mild form of SIOD. A 14.5-year-old male patient presented with disproportionate short stature, SRNS (focal and segmental glomerulosclerosis), laboratory evidence of cellular immune deficiency and radiologic characteristics of SED. He died at the age of 16.5 years with bone marrow failure and severe pneumonia. To the best of our knowledge, this is the first case of SIOD to be reported from Egypt.Entities:
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Year: 2015 PMID: 26354575 DOI: 10.4103/1319-2442.164585
Source DB: PubMed Journal: Saudi J Kidney Dis Transpl ISSN: 1319-2442