Suppr超能文献

先天性轴后纵向肢体缺损的产前诊断:一例报告

Prenatal diagnosis of a congenital postaxial longitudinal limb defect: a case report.

作者信息

Pauleta Joana, Melo Maria Antonieta, Graça Luís Mendes

机构信息

Ultrasound Unit, Department of Obstetrics, Gynecology and Reproductive Medicine, Santa Maria University Hospital, 1649-035 Lisbon, Portugal.

出版信息

Obstet Gynecol Int. 2010;2010:825639. doi: 10.1155/2010/825639. Epub 2010 May 30.

Abstract

Introduction. Although congenital longitudinal fibular deficiency is one of the most common long bone deficiencies, there are few published cases of its prenatal diagnosis. Case report. A right longitudinal deficiency of the fibula associated with tibial shortening, foot equinovalgus, and absence of the fourth and fifth foot rays diagnosed at 22 weeks gestation is described. Sequential ultrasonographic surveillance was performed without obstetric complications. The anomaly was confirmed after birth, and conservative orthopaedic management was decided. Conclusion. Though rarely seen, postaxial longitudinal limb defect may be detected by ultrasound. The correct approach can only be decided after birth, when the functional impact of the anomaly can be fully evaluated.

摘要

引言。尽管先天性腓骨纵向缺如属于最常见的长骨缺如之一,但关于其产前诊断的已发表病例却很少。病例报告。本文描述了一例妊娠22周时诊断出的右侧腓骨纵向缺如,伴有胫骨缩短、马蹄外翻足以及第四和第五足趾缺如。在无产科并发症的情况下进行了连续超声监测。出生后证实了该异常情况,并决定采取保守的骨科治疗方法。结论。虽然轴后纵向肢体缺损很少见,但超声检查可能会检测到。只有在出生后,当能够全面评估该异常对功能的影响时,才能确定正确的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/233b/2878671/ed4d94cc114d/OGI2010-825639.001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验