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眼耳脊椎(戈尔登哈综合征)复合体中的严重轴向异常。

Severe axial anomalies in the oculo-auriculo-vertebral (Goldenhar) complex.

作者信息

Ignacio Rodríguez J, Palacios J, Lapunzina P

机构信息

Department of Pathology, La Paz Hospital, Madrid, Spain.

出版信息

Am J Med Genet. 1993 Aug 1;47(1):69-74. doi: 10.1002/ajmg.1320470115.

Abstract

We have studied 4 infants with oculo-auriculo-vertebral (OAV) complex or Goldenhar "syndrome" who also had severe axial anomalies, including multiple vertebral segmentation errors affecting the thoracic and the lumbar spine. One of them presented a previously unreported pattern of vertebral and rib anomalies similar to spondylocostal dysostosis. Three patients had twins, and all 4 patients had other associated non-skeletal malformations which affected the midline, i.e., cleft lip and palate, esophageal atresia with tracheoesophageal fistula, and ventricular septal defect. The broad extent of the axial anomalies, the association with midline defects and twinning, and the combination in the same patient of two distinct conditions support the concept that OAV complex is a polytopic developmental field defect arising during blastogenesis.

摘要

我们研究了4例患有眼-耳-脊椎(OAV)复合体或Goldenhar“综合征”的婴儿,他们还伴有严重的脊柱异常,包括影响胸椎和腰椎的多个椎体节段性异常。其中1例呈现出一种先前未报道过的椎体和肋骨异常模式,类似于脊椎肋骨发育不良。3例患者有双胞胎,所有4例患者都有其他相关的非骨骼畸形,这些畸形影响中线结构,即唇腭裂、食管闭锁合并气管食管瘘和室间隔缺损。轴向异常的广泛程度、与中线缺陷和双胎妊娠的关联,以及同一患者中两种不同情况的组合,支持了OAV复合体是一种在胚胎发育早期发生的多部位发育场缺陷的概念。

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