Haddad R, Uwaydat S, Dakroub R, Traboulsi E I
Department of Ophthalmology, American University of Beirut Medical Center, Beirut, Lebanon.
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.
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.
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。