| Literature DB >> 12910495 |
Carsten Bergmann1, Klaus Zerres, Thomas Peschgens, Jan Senderek, Helmut Hörnchen, Sabine Rudnik-Schöneborn.
Abstract
We describe a male infant born to consanguineous healthy parents with multiple congenital anomalies of the skeleton and internal organs. His phenotype displays an overlap between VACTERL and hemifacial microsomia (oculo-auriculo-vertebral spectrum/OAV). In addition, striking asymmetry of the malformations further supports the classification as part of the "axial mesodermal dysplasia complex" (AMDC) which is supposed to arise from disturbed mesodermal cell migration during early blastogenesis. The present case was instructive to review the continuous spectrum of AMDC related anomalies. Copyright 2003 Wiley-Liss, Inc.Entities:
Mesh:
Year: 2003 PMID: 12910495 DOI: 10.1002/ajmg.a.20167
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802