Suppr超能文献

晶状体异位和独特颅面外观的常染色体隐性综合征的确诊。

Confirmation of the autosomal recessive syndrome of ectopia lentis and distinctive craniofacial appearance.

作者信息

Haddad R, Uwaydat S, Dakroub R, Traboulsi E I

机构信息

Department of Ophthalmology, American University of Beirut Medical Center, Beirut, Lebanon.

出版信息

Am J Med Genet. 2001 Mar 15;99(3):185-9. doi: 10.1002/1096-8628(2001)9999:9999<::aid-ajmg1156>3.0.co;2-v.

Abstract

We report four members of a Lebanese Druze family with the syndrome of lens dislocation, spontaneous filtering blebs, anterior segment abnormalities, and a distinctive facial appearance. The constellation of clinical abnormalities in these patients is not suggestive of the Marfan syndrome or other connective tissue disorders associated with ectopia lentis. We previously described this syndrome in another presumably unrelated and highly inbred Druze family from the mountains of Lebanon. We postulated autosomal recessive inheritance in a pseudo-dominant pedigree. A few isolated reports of similar cases are scattered in the world literature. We now confirm that this is a distinct autosomal recessive syndrome whose gene mutation is enriched in the Lebanese Druze community.

摘要

我们报告了一个黎巴嫩德鲁兹家族的四名成员,他们患有晶状体脱位、自发性滤过泡、眼前段异常以及独特的面部外观综合征。这些患者的一系列临床异常并不提示马凡综合征或其他与晶状体异位相关的结缔组织疾病。我们之前在另一个可能无亲缘关系且高度近亲结婚的黎巴嫩山区德鲁兹家族中描述过这种综合征。我们推测在一个假显性系谱中为常染色体隐性遗传。世界文献中零散分布着一些类似病例的单独报告。我们现在证实这是一种独特的常染色体隐性综合征,其基因突变在黎巴嫩德鲁兹社区更为常见。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验