A case of familial syndactyly associated with eye and dental abnormalities

被引：2
|
作者：
Mills, Janith K. [1 ]
Wheeler, Lesley [2 ,3 ]
Oishi, Scott N. [2 ,3 ]
机构：
[1] Texas Scottish Rite Hosp Children, Hand Ctr, Dallas, TX 75219 USA
[2] Univ Texas SW Med Ctr Dallas, Dept Orthoped Surg, Dallas, TX 75390 USA
[3] Univ Texas SW Med Ctr Dallas, Dept Plast Surg, Dallas, TX 75390 USA
来源：
JAAPA-JOURNAL OF THE AMERICAN ACADEMY OF PHYSICIAN ASSISTANTS | 2015年 / 28卷 / 12期
关键词：
syndactyly; clinodactyly; oculodentodigital dysplasia; dental abnormalities; familial; autosomal dominant; OCULODENTODIGITAL DYSPLASIA; GJA1; MUTATIONS; PHENOTYPE;
D O I：
10.1097/01.JAA.0000471611.99902.fe
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
Syndactyly occurs in 1 in 2,000 live births and is more common in white children. This article describes a patient with syndactyly and additional abnormalities indicating oculodentodigital dysplasia.
引用
收藏
页码：40 / 43
页数：4
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