| Literature DB >> 2253248 |
A J Barakat1, P Arianas, A D Glick, M G Butler.
Abstract
We report a 6-year-old white male with Laurence-Moon-Biedl syndrome and focal sclerosing glomerulonephritis (FSGN). To our knowledge, FSGN has not been reported previously in patients with this syndrome. We wish to alert the clinician to the wide variety of renal abnormalities that can be seen in patients with this rare, autosomal recessive disorder.Entities:
Mesh:
Year: 1990 PMID: 2253248 PMCID: PMC6697078
Source DB: PubMed Journal: Child Nephrol Urol ISSN: 1012-6694