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锁骨颅骨发育不全的产前诊断。

Prenatal diagnosis of cleidocranial dysostosis.

作者信息

Hamner L H, Fabbri E L, Browne P C

机构信息

Department of Gynecology and Obstetrics, Emory University School of Medicine, Atlanta, Georgia.

出版信息

Obstet Gynecol. 1994 May;83(5 Pt 2):856-7.

PMID:8159376
Abstract

BACKGROUND

Cleidocranial dysostosis is an autosomal dominant disorder characterized by absent or hypoplastic clavicles and dysplasia of the osseous tissue in the cranium.

CASE

We describe the prenatal diagnosis and neonatal evaluation of cleidocranial dysostosis in the pregnancy of a woman also affected with this disorder.

CONCLUSION

The sonographic appearance of absent or hypoplastic clavicles, in the absence of other findings suggesting a skeletal dysplasia, strongly suggests the diagnosis of cleidocranial dysostosis. Nomograms are available to follow the growth and development of normal clavicles. Assessment of normal long-bone growth in relation to clavicular size may aid in the diagnosis.

摘要

背景

锁骨颅骨发育不全是一种常染色体显性疾病,其特征为锁骨缺失或发育不全以及颅骨骨组织发育异常。

病例

我们描述了一名患有该疾病的孕妇的锁骨颅骨发育不全的产前诊断及新生儿评估情况。

结论

在无其他提示骨骼发育异常的表现时,超声检查显示锁骨缺失或发育不全强烈提示锁骨颅骨发育不全的诊断。有用于跟踪正常锁骨生长发育的列线图。评估正常长骨生长与锁骨大小的关系可能有助于诊断。

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