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先天性肩胛盂发育不良:连续两代的病例报告。

Congenital glenoid dysplasia: case report in two consecutive generations.

作者信息

Stanciu C, Morin B

机构信息

Orthopedic Department, Hôpital Sainte-Justine Montreal, Quebec, Canada.

出版信息

J Pediatr Orthop. 1994 May-Jun;14(3):389-91. doi: 10.1097/01241398-199405000-00025.

Abstract

Congenital glenoid dysplasia is a rare congenital condition of the shoulder. We report the case of a 6-year-old girl that was referred to our institution for restricted motion of both shoulders. Radiological examination revealed bilateral glenoid dysplasia. At the time of the child's examination, her mother also complained of shoulder stiffness; radiographs of her shoulders were taken and revealed that she too had glenoid dysplasia. Congenital glenoid dysplasia results from failure of development of the inferior ossification center of the glenoid fossa. Shoulder stiffness is the primary resultant disability, although it is variable. Our case is notable because we identified the dysplasia in two successive generations of the same family, although the mother was unaware she had the condition.

摘要

先天性肩胛盂发育不良是一种罕见的肩部先天性疾病。我们报告了一名6岁女孩的病例,她因双肩活动受限被转诊至我院。放射学检查显示双侧肩胛盂发育不良。在对该患儿进行检查时,其母亲也诉说肩部僵硬;对她的肩部进行了X线检查,结果显示她也患有肩胛盂发育不良。先天性肩胛盂发育不良是由于肩胛盂下骨化中心发育失败所致。肩部僵硬是主要的致残后果,不过其程度因人而异。我们的病例值得关注,因为我们在同一家庭的两代人中发现了这种发育不良,尽管母亲并未意识到自己患有该疾病。

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