腰骶肋椎综合征伴发 VACTERL 异常：一例新生儿病例报告。

Lumbocostovertebral syndrome with associated VACTERL anomalad: a neonatal case report.

机构信息

Department of Pediatrics, University of Kansas School of Medicine, Wichita-Carriage Parkway, Wichita, KS 67208, USA.

出版信息

J Perinatol. 2009 Dec;29(12):826-7. doi: 10.1038/jp.2009.82.

DOI:10.1038/jp.2009.82

PMID:19935732

Abstract

We report the first clinical case of a term infant with findings suggestive of lumbocostovertebral syndrome and VACTERL association. Renal agenesis was suspected by prenatal ultrasound, and at birth clinical findings included a large abdominal wall hernia, imperforate anus, vestibular fistula, absent right rib, vertebral anomalies, tethered cord, syringomyelia, and two small sacral dimples.

摘要

我们报告了首例足月婴儿的临床病例，其表现提示存在腰骶肋椎畸形综合征和 VACTERL 联合征。产前超声怀疑存在肾发育不全，出生时的临床发现包括巨大的腹壁疝、肛门闭锁、前庭瘘、右侧肋骨缺失、椎体异常、脊髓栓系、脊髓空洞症和两个小的骶尾部凹陷。