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成骨不全合并先天性多发性关节挛缩症(布鲁克综合征)——可能为常染色体隐性遗传的证据

Osteogenesis imperfecta with arthrogryposis multiplex congenita (Bruck syndrome)--evidence for possible autosomal recessive inheritance.

作者信息

Brady A F, Patton M A

机构信息

Department of Medical Genetics, St George's Hospital Medical School, London, UK.

出版信息

Clin Dysmorphol. 1997 Oct;6(4):329-36. doi: 10.1097/00019605-199710000-00005.

Abstract

We report a son and a daughter of a first cousin Pakistani marriage who both have osteogenesis imperfecta and the son in addition has arthrogryposis multiplex congenita. Bruck [(1897): Dtsch Med Wochenschr 23: 152-155] first reported the case of a boy who had multiple fractures and joint ankylosis, subsequently only one sibship with three affected cases and seven sporadic cases have been reported to our knowledge. On the basis of consanguinity this suggests that the association of osteogenesis imperfecta and arthrogryposis multiplex congenita is inherited in this family as an autosomal recessive condition with variable expression.

摘要

我们报告了一对巴基斯坦近亲结婚夫妇的儿子和女儿,他们都患有成骨不全症,并且儿子还患有先天性多发性关节挛缩症。布鲁克(1897年)首次报道了一名患有多处骨折和关节强直的男孩病例,据我们所知,随后仅报道了一个有三例患者的同胞家族和七例散发病例。基于近亲关系,这表明在这个家族中,成骨不全症与先天性多发性关节挛缩症的关联是以常染色体隐性疾病的形式遗传的,且表现形式多样。

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