Halal F, Farsky K
Am J Med Genet. 1981;8(1):53-8. doi: 10.1002/ajmg.1320080107.
We report a five-year-old boy with bilateral ocular coloboma, hypertelorism, hypospadias, and mental retardation. The father has hypertelorism and a deceased sibling had unilateral iris coloboma. This observation my represent 1) the BBB syndrome with coincidentally segregating coloboma; 2) discovery of coloboma as a new but rare component manifestation of the BBB syndrome; or 3) a new autosomal dominant pleiotropic syndrome.
我们报告了一名患有双侧眼裂、眼距过宽、尿道下裂和智力发育迟缓的5岁男孩。父亲有眼距过宽,一个已故的兄弟姐妹患有单侧虹膜裂。这一观察结果可能代表:1)伴有巧合性分离性裂的BBB综合征;2)发现裂是BBB综合征一种新的但罕见的组成部分表现;或3)一种新的常染色体显性多效性综合征。