| Literature DB >> 12808682 |
Abstract
We describe a case of first-trimester diagnosis of micrognathia. A transvaginal ultrasound scan performed at 13 weeks' gestation revealed an abnormal fetal facial profile consisting of a small mandible and a receding chin. A subsequent amniocentesis at 15 weeks' gestation revealed a normal karyotype. A morphology scan and subsequent postmortem examination at 19 weeks confirmed the first-trimester findings and revealed, in addition to the facial pathology, a complex cardiac abnormality and unilateral talipes equinovarus. These findings are consistent with the diagnosis of Pierre Robin syndrome. Copyright 2003 ISUOG. Published by John Wiley & Sons, Ltd.Entities:
Mesh:
Year: 2003 PMID: 12808682 DOI: 10.1002/uog.141
Source DB: PubMed Journal: Ultrasound Obstet Gynecol ISSN: 0960-7692 Impact factor: 7.299