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多发性骨骺发育不良的X线诊断:附家族性发病三例分析 总被引:2,自引:0,他引:2
This is a case report of 3 cases from the same family with multiple epiphyseal dysplasia. The disease is an uncommon congenital dominant hereditary disease of the bone characterized by multiple and symmetrical skeletal involvement with retardation of epiphyseal development, accompanied by irregularity and shortening of toes and fingers and yet still maintaining the normal proportion between the trunk and extremities. The intelligence is not affected. In the adult patients, sloping of distal tibial articular surface associated with degenerative changes of both hip joints is a reliable diagnostic sign. The aforementioned X-ray signs are helpful to distinguish this condition from other chondrodysplasia diseases. 相似文献
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近年来笔者采用X线诊断假性痛风 6例 ,现报告如下。1 临床资料本组 6例均为男性。年龄 1 9~ 73岁。病史8个月~ 1 2年。临床症状多以疼痛为主 ,1例有双膝关节疼痛 ,2例为双膝、踝、肘关节痛 ,另 3例除包括对称的髋、肩、肘、踝、腕关节外 ,还有腰椎的多关节多部位疼痛。疼痛多为突发性、无规律的急性发作 ,发作时可有膝、踝关节轻度肿胀 ,4例有膝关节轻度红肿热 ,3例有轻度膝、髋、肘关节活动受限。5例经左膝关节镜检查示关节液非脓性 ,关节面尚光滑 ,可见软骨表面点状或线状闪光的白色钙斑 ,其中 2例关节液中找到二羟焦磷酸钙结晶。 1例… 相似文献
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