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先天性脊椎骨骺发育不良的两种临床变异型。

Two clinical variants of spondylo-epiphysial dysplasia congenita.

作者信息

Wynne-Davies R, Hall C

出版信息

J Bone Joint Surg Br. 1982;64(4):435-41. doi: 10.1302/0301-620X.64B4.6807992.

Abstract

Seventeen patients with congenital spondylo-epiphysial dysplasia from six centres in Britain have been investigated and two variants delineated. There is wide clinical and radiological variability in each group with overlap between them, but 12 of the patients had very short stature and grossly disorganised hips with severe coxa vara, and the five remaining patients were less seriously affected with height only a little below the third percentile and only mild coxa vara. Both groups can be diagnosed at birth but the two cannot be differentiated on clinical and radiological grounds until after the age of three to four years when the developing severe coxa vara and difference in stature become apparent. All cases were sporadic with the exception of a concordant twin-pair.

摘要

来自英国六个中心的17例先天性脊椎骨骺发育不良患者接受了调查,并确定了两种变异型。每组患者在临床和影像学上都存在很大差异,两组之间有重叠,但其中12例患者身材极矮,髋关节严重紊乱,伴有严重的髋内翻,其余5例患者受影响较轻,身高仅略低于第三百分位,只有轻度髋内翻。两组患者在出生时均可诊断,但在3至4岁之前,根据临床和影像学依据无法区分两者,此时严重的髋内翻和身高差异才会显现出来。除一对同卵双胞胎外,所有病例均为散发性。

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