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首页> 外文期刊>Obstetrics and Gynecology International >Prenatal Diagnosis of a Congenital Postaxial Longitudinal Limb Defect: A Case Report
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Prenatal Diagnosis of a Congenital Postaxial Longitudinal Limb Defect: A Case Report

机译:先天性后轴纵向肢体缺陷的产前诊断:病例报告。

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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.
机译:介绍。尽管先天性纵向腓骨缺乏症是最常见的长骨缺乏症之一,但其产前诊断的已发表病例很少。描述了腓骨的右纵向缺乏症,与胫骨缩短,足等脚趾畸形有关,并且在妊娠22周时没有诊断出第四和第五只足部射线。连续超声检查无产科并发症。出生后确认异常,并决定保守骨科治疗。结论。虽然很少见,但可以通过超声检测到后轴纵肢缺损。只有能够完全评估异常的功能影响,才能在出生后确定正确的方法。

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