| Literature DB >> 3812578 |
F Greenberg, M V Gresik, R J Carpenter, S W Law, L P Hoffman, D H Ledbetter.
Abstract
We report on two sib fetuses with similar abnormalities detected prenatally by ultrasound. The first fetus had micrognathia, was without cleft palate, and had low-set ears, double outlet right ventricle with a ventricular septal defect, and 46,XY gonadal dysgenesis. The second sib fetus was born with cleft lip and palate, micrognathia, transposition of the great vessels, ventricular septal defect, a right-sided aorta arch, and bilateral cystic kidneys with hypospadias. We were able to identify 11 additional cases in the literature with similar findings. We think this set of defects is a recognizable syndrome that appears to be inherited either as an autosomal recessive or as an X-linked recessive and may overlap with the Smith-Lemli-Opitz syndrome.Entities:
Mesh:
Year: 1987 PMID: 3812578 DOI: 10.1002/ajmg.1320260111
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299