Literature DB >> 26354575

Schimke immune-osseous dysplasia: A case report.

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.

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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


  1 in total

1.  Schimke Immuno-osseous Dysplasia: A Case Report.

Authors:  Amir Hossein Babaei; Soroor Inaloo; Mitra Basiratnia
Journal:  Indian J Nephrol       Date:  2019 Jul-Aug
  1 in total

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