| Literature DB >> 2248295 |
Abstract
We report on an infant with bilateral ulnar agenesis, radial hypoplasia, oligodactyly, hydrops fetalis, and endocardial fibroelastosis (EFE). The presence of the 2 major malformations and parental consanguinity suggests the possibility of a new autosomal recessive MCA syndrome.Entities:
Mesh：
Year: 1990 PMID： 2248295 DOI： 10.1002/ajmg.1320370219
Source DB: PubMed Journal: Am J Med Genet ISSN： 0148-7299