Overlap between VACTERL and hemifacial microsomia illustrating a spectrum of malformations seen in axial mesodermal dysplasia complex (AMDC)

被引:29
作者
Bergmann, C
Zerres, K
Peschgens, T
Senderek, J
Hörnchen, H
Rudnik-Schöneborn, S
机构
[1] Rhein Westfal TH Aachen, Inst Human Genet, D-52074 Aachen, Germany
[2] Rhein Westfal TH Aachen, Dept Pediat, Neonatal Intens Care Unit, D-52074 Aachen, Germany
关键词
axial mesodermal dysplasia complex; primary developmental field defect; VACTERL; hemifacial microsomia; oculo-auriculovertebral spectrum (OAV);
D O I
10.1002/ajmg.a.20167
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:151 / 155
页数:5
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