Stewart F J, Nevin N C, Brown S
Department of Medical Genetics, Belfast City Hospital, Northern Ireland.
Am J Med Genet. 1993 Feb 15;45(4):426-9. doi: 10.1002/ajmg.1320450405.
We report on a 4-month-old boy with manifestations of both the oculo-auriculovertebral spectrum and the caudal regression sequence. He has preauricular appendages, thoracic and lumbar hemivertebrae, anomalies of the ribs, dextrocardia, sacral "dysplasia," dislocated hips, bilateral talipes equinovarus, imperforate anus, recto-vesical fistula, malformed scrotum, and undescended testes. As suggested by Russell et al. [1981], who reported a patient with similar anomalies, the spectrum of anomalies probably is due to a generalized alteration in mesodermal cell migration during the primitive streak period. The term "axial mesodermal dysplasia spectrum" best describes the widespread anomalies in the cranial and caudal regions.
我们报告了一名4个月大的男婴,他同时具有眼-耳-脊椎综合征和尾端退化序列的表现。他有耳前附件、胸腰椎半椎体、肋骨异常、右位心、骶骨“发育不良”、髋关节脱位、双侧马蹄内翻足、肛门闭锁、直肠膀胱瘘、阴囊畸形和隐睾。正如Russell等人[1981年]所报道的一名有类似异常的患者,这种异常谱可能是由于原条期期间中胚层细胞迁移的普遍改变所致。“轴性中胚层发育异常谱”这一术语最能描述头侧和尾侧区域广泛存在的异常。