| Literature DB >> 6846397 |
R Carmi, M Binshtock, D Abeliovich, J Bar-Ziv.
Abstract
We report a man who had the branchio-oto-renal (BOR) syndrome with crossed renal ectopia. His three children were born with bilateral renal agenesis and the so-called Potter syndrome. This case illustrates the potential severity of the renal anomalies in the BOR syndrome and the inadequacy of oligohydramnios and maternal serum alpha-fetoprotein as screening methods for renal agenesis. This case also implies strongly the necessity for meticulous search for renal anomalies in individuals with the BOR syndrome and proper counseling regarding the possibility of lethal bilateral renal agenesis.Entities:
Mesh:
Year: 1983 PMID: 6846397 DOI: 10.1002/ajmg.1320140405
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299