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Results of deformity correction in children with X-linked hereditary hypophosphatemic rickets by external fixation or combined technique

机译:X-连锁遗传性低磷酸盐血症性by病儿童外固定或联合矫正畸形的结果

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Background The operative procedures to correct multiplanar bone deformities may be indicated for prevention of secondary orthopaedic complications in children with X-linked hereditary hypophosphatemic rickets (XHPR). Different problems related to surgical correction were reported: increased rate of non-union, delayed union, recurrent deformity, deep intramedullary infection, refracture, nerve palsy, and pin tract infection. The aim of this retrospective study was comparison of results of correction in children with XHPR who underwent the treatment with either the Ilizarov device alone or a combined technique: the Ilizarov fixator with flexible intramedullary nailing (FIN) with hydroxyapatite bioactive coating and FIN.
机译:背景技术可能需要纠正多平面骨畸形的手术程序,以预防X连锁遗传性低磷酸盐血症性rick病(XHPR)儿童的继发性骨科并发症。报道了与手术矫正相关的不同问题:不愈合率增加,愈合延迟,复发畸形,深部髓内感染,再狭窄,神经性麻痹和针道感染。这项回顾性研究的目的是比较XHPR患儿的矫正结果,这些患儿单独使用Ilizarov装置或联合技术进行了治疗:带柔性羟基磷灰石生物活性涂层和FIN的Ilizarov固定器与柔性髓内钉(FIN)。

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