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[尾椎退化综合征 - 尾椎发育不全]

[Caudal regression syndrome - caudal agenesis].

作者信息

van Baalen A, Jacobs J, Alfke K, Caliebe A, Stephani U

机构信息

Klinik für Neuropädiatrie, Universitätsklinikum Schleswig-Holstein, Christian-Albrechts-Universität zu Kiel, Kiel, Germany.

出版信息

Klin Padiatr. 2008 Mar-Apr;220(2):86-7. doi: 10.1055/s-2007-993193. Epub 2007 Dec 21.

Abstract

BACKGROUND

Neural tube defects are caused by complex genetic and environmental factors. The congenital anomaly most specific to pregnant women with diabetes mellitus is caudal regression syndrome.

PATIENT

A 4-year-old boy with a history of mild delay in motor development presented with primary enuresis and encopresis. On physical examination, he had no sensory and motor deficits, but a short anal cleft. On questioning, the mother reported insulin-dependent diabetes mellitus during pregnancy. MRI of the spinal cord demonstrated a thoracic syringomyelia, a dysplastic conus medullaris, and an absence of coccyx and distal sacrum, called caudal regression syndrome or caudal agenesis.

CONCLUSION

The caudal regression syndrome refers to sacral agenesis associated with spinal cord anomalies, e.g. syringomyelia. Sacral agenesis is marked by total absence of the coccyx and total or distal absence of the sacrum. An abnormal backside combined with a history of maternal diabetes mellitus in pregnancy is highly suggestive for the presence of caudal regression syndrome.

摘要

背景

神经管缺陷由复杂的遗传和环境因素引起。糖尿病孕妇最具特异性的先天性异常是尾椎退化综合征。

患者

一名4岁男孩,有运动发育轻度延迟史,出现原发性遗尿和遗粪症。体格检查时,他无感觉和运动缺陷,但肛门裂短。经询问,母亲报告孕期患有胰岛素依赖型糖尿病。脊髓磁共振成像显示胸段脊髓空洞症、发育异常的圆锥和尾骨及远端骶骨缺如,称为尾椎退化综合征或尾骨发育不全。

结论

尾椎退化综合征指与脊髓异常(如脊髓空洞症)相关的骶骨发育不全。骶骨发育不全的特征是尾骨完全缺如以及骶骨完全或远端缺如。背部异常加上孕期母亲糖尿病史高度提示存在尾椎退化综合征。

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