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Familial osteochondritis dissecans associated with early osteoarthritis and disproportionate short stature.

机译:家族性骨软骨炎剥离与早期骨关节炎相关,且身材矮小。

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OBJECTIVE: Familial osteochondritis dissecans (OCD) is a rare disorder characterised by disturbed chondro-skeletal development, disproportionate growth and deformation of the skeleton. DESIGN: We identified a five-generation family with 15 living affected members from Northern Sweden. The disorder was diagnosed with a case definition of OCD in at least one joint. RESULTS: Main clinical findings consisted of OCD in knees and/or hips and/or elbows, disproportionate short stature and early osteoarthritis (OA). There were no radiological indications of epiphyseal dysplasia. Anthropometric measurements of affected individuals showed short stature, a high ratio between sitting height and total height, a relatively normal arm span and head circumference. In 12 of 15 cases, onset was during late childhood or adolescence and OA had developed in seven of those patients. CONCLUSIONS: Our observation suggests that OA is a frequent complication in familial OCD even though the lesions appear before closure of physis.
机译:目的:家族性剥离性骨软骨炎(OCD)是一种罕见的疾病,其特征是软骨骨骼发育紊乱,骨骼生长和变形不均衡。设计:我们确定了一个五代家庭,其中有15名来自瑞典北部的在世居民。该疾病至少在一个关节中被诊断为强迫症。结果:主要临床发现包括膝部和/或臀部和/或肘部的强迫症,不成比例的矮小身材和早期骨关节炎(OA)。没有骨epi发育异常的放射学指征。对受影响个体的人体测量显示身材矮小,坐高与总高之比高,手臂跨度和头围相对正常。 15例中有12例发病于儿童晚期或青春期,其中7例发生了OA。结论:我们的观察表明,OA是家族性OCD的一种常见并发症,即使病变出现在物理闭合之前。

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