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[罕见的家族性迟发性股骨头骨骺溶解病例]

[Unusual familial case of epiphyseolysis capitis femoris lenta].

作者信息

Montskó P, Dejonge T

出版信息

Magy Traumatol Ortop Kezseb Plasztikai Seb. 1994;37(1):89-91.

PMID:8162145
Abstract

A rare case of familial slipped capital femoral epiphysis is discussed. Of total five siblings four were affected. All the cases, except one boy, were treated in the Orthopaedic Department of the Medical University Pécs. The fourth affected child was treated conservatively because of the consecutive osteoarthritis, the other three were treated operatively. The literature is reviewed. The possible etiological factors are discussed emphasizing the role of heredity and it can be concluded that the endocrine constitution predisposing to epiphyseolysis be hereditary.

摘要

本文讨论了一例罕见的家族性股骨头骨骺滑脱病例。在五个兄弟姐妹中,有四个患病。除一名男孩外,所有病例均在佩奇医科大学骨科接受治疗。第四名患病儿童因并发骨关节炎而接受保守治疗,另外三名则接受了手术治疗。本文对相关文献进行了综述,并讨论了可能的病因,强调了遗传因素的作用。可以得出结论,易发生骨骺溶解的内分泌体质可能具有遗传性。

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