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[一名患有II型显性胶原病女孩的髋关节发育不良和脊柱骨软骨炎(休曼病)]

[Hip dysplasia and spinal osteochondritis (Scheuermann's disease) in a girl with type II manifesting collagenopathy].

作者信息

Al Kaissi A, Laccone F, Karner C, Ganger R, Klaushofer K, Grill F

机构信息

Ludwig Boltzmann Institute of Osteology, Hanusch Hospital, Heinrich-Collin-Str. A-30, 1140, Wien, Österreich,

出版信息

Orthopade. 2013 Nov;42(11):963-8. doi: 10.1007/s00132-013-2182-1.

DOI:10.1007/s00132-013-2182-1
PMID:24013370
Abstract

OBJECTIVES

This paper describes the natural course of irritable hip pain associated with spinal rigidity and pain in the thoracic region with subsequent development of mild kyphosis in a girl with a mutation in the collagen 2 alpha 1 gene (type II collagenopathy).

METHODS

Phenotypic and genotypic characterization was carried out in a 14-year-old girl to identify the underlying pathology of severe irritable hip pain associated with thoracic spinal rigidity and pain. Detailed clinical examination, skeletal survey and genetic testing were performed accordingly. Bernese periacetabular osteotomy was used to alleviate pain and to improve the anatomical correlation of the acetabular and femoral heads.

RESULTS

Short stature associated with acetabulo-femoral dysplasia, spinal osteochondritis (Scheuermann's disease) and mild thoracic kyphosis were the most prominent abnormalities. Genetic analysis showed a heterozygous mutation in the collagen type II gene (COL2A1-c.1636G>A, p. G546S). A Bernese periacetabular osteotomy was performed to improve the clinical status of the patient. There was significant improvement in the extrusion index, the acetabular index and the lateral center-edge angle.

CONCLUSIONS

Hip dysplasia and Scheuermann's osteochondritis have never been reported in connection with a mutation in COL2A1 (collagenopathy type II). Awareness is needed for careful phenotypic and genotypic characterization in patients with irritable hip pain and spinal stiffness.

摘要

目的

本文描述了一名患有Ⅱ型胶原病(胶原蛋白2α1基因突变)的女孩,其与脊柱僵硬和胸段疼痛相关的易激惹性髋关节疼痛的自然病程,以及随后出现的轻度脊柱后凸。

方法

对一名14岁女孩进行表型和基因型特征分析,以确定与胸段脊柱僵硬和疼痛相关的严重易激惹性髋关节疼痛的潜在病理。相应地进行了详细的临床检查、骨骼检查和基因检测。采用伯尔尼髋臼周围截骨术来缓解疼痛,并改善髋臼和股骨头的解剖关系。

结果

身材矮小伴髋臼股骨发育不良、脊柱骨软骨炎(休门氏病)和轻度胸段脊柱后凸是最突出的异常表现。基因分析显示Ⅱ型胶原基因(COL2A1-c.1636G>A,p.G546S)存在杂合突变。实施了伯尔尼髋臼周围截骨术以改善患者的临床状况。挤压指数、髋臼指数和外侧中心边缘角有显著改善。

结论

COL2A1突变(Ⅱ型胶原病)相关的髋关节发育不良和休门氏骨软骨炎此前未见报道。对于易激惹性髋关节疼痛和脊柱僵硬的患者,需要通过仔细的表型和基因型特征分析来提高认识。

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Recurrent c.G1636A (p.G546S) mutation of COL2A1 in a Chinese family with skeletal dysplasia and different metaphyseal changes: a case report.

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Radiographic and tomographic analysis in patients with stickler syndrome type I.I 型斯特奇-韦伯综合征患者的影像学分析
Int J Med Sci. 2013 Aug 3;10(9):1250-8. doi: 10.7150/ijms.4997. Print 2013.
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