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两例戈洛普-沃尔夫冈复合体膝关节离断术后的5年随访研究。

A 5-year follow-up study after knee disarticulation in two cases of Gollop-Wolfgang complex.

作者信息

Bos Cees F A, Taminiau Antonie H M

机构信息

Department of Pediatric Orthopaedic Surgery, Leiden University Medical Center, Location Juliana Children's Hospital, MJ Den Haag, The Netherlands.

出版信息

J Pediatr Orthop B. 2007 Nov;16(6):409-13. doi: 10.1097/BPB.0b013e3282f057f3.

Abstract

The Gollop-Wolfgang Complex is a very rare anomaly, which has its essential features in congenital absence of the tibia and ipsilateral bifurcation of the femur. Surgical treatment of two patients with a follow-up of 5 years is reported.

摘要

戈洛普-沃尔夫冈复合体是一种非常罕见的畸形,其主要特征是先天性胫骨缺如和同侧股骨分叉。本文报道了对两名患者进行手术治疗并随访5年的情况。

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