| Literature DB >> 32341815 |
Esra Nagehan Akyol Onder1, Mine Ozkol2, Nalan Nese3, Can Taneli4, Osman Orkun Cankorur5, Ipek Ozunan1.
Abstract
Xanthogranulomatous pyelonephritis (XGP) is characterized by destruction of the renal parenchyma and granulomatous inflammation with lipid-laden foamy macrophages as well as inflammatory infiltration and intensive renal fibrosis. It generally occurs in adults, especially those in the fifth and sixth decades of life, but is occasionally seen in children as well. Brachydactyly mental retardation (BDMR) syndrome (OMIM 600430) is caused by a small deletion of chromosome 2q37 and is a rare condition, with roughly 100 cases reported worldwide. Here, we describe the case of a patient with deletion of chromosome 2q37, which is known as the BDMR syndrome, and XGP. © Thieme Medical Publishers.Entities:
Keywords: 2q37 deletion syndrome; brachydactyly mental retardation syndrome; xanthogranulomatous pyelonephritis
Year: 2019 PMID: 32341815 PMCID: PMC7183408 DOI: 10.1055/s-0039-1697624
Source DB: PubMed Journal: J Pediatr Genet ISSN: 2146-460X