Syndrome of telecanthus, hypertelorism, strabismus, and pes cavus in father and son
Syndrome of telecanthus, hypertelorism, strabismus, and pes cavus in father and son
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父子患有远眦症、远距症、斜视、高弓足综合征
DOI：
10.1002/ajmg.1320200119
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发表时间：
1985
期刊：
影响因子：
--
通讯作者：
J. Reynolds
中科院分区：
文献类型：
--
作者：
C. Krauss;T. Herman;L. Holmes;J. M. Opitz;J. Reynolds
我们报告了一对患有远距花、多角症、斜视和下丘脑的父子。此外，儿子还患有尿道下裂、双侧腹股沟疝气、双侧指侧斜指和双侧喜指，鼻尖有小组织肿块，放射学表现包括长骨干骺端张开和骨质减少。
We report on a father and son who have telecanthus, hypertelorism, strabismus, and pes cavus. In addition, the son has hypospadias, bilateral inguinal hernia, clinodactyly and camptodactyly of fingers bilaterally, a small tissue mass on the tip of his nose, and radiographic findings including flared metaphyses of long bones and osteopenia.