Epiphyseal osteochondromas with autosomal dominant inheritance and multiple parosteal bone proliferations

被引:5
作者
Fahmy, Mohamed A. L.
Pandey, Tarun
机构
[1] Univ Arkansas Med Sci, Dept Radiol, Little Rock, AR 72205 USA
[2] Razi Orthoped Hosp, Safat 13043, Kuwait
关键词
carpotarsal osteochondromatosis; dominant; dysplasia epiphysealis hemimelica; osteochondromas;
D O I
10.1007/s00256-007-0394-3
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
The familial cases of dysplasia epiphysealis hemimelica (DEH), or Trevor's disease, are thought to represent dominant carpotarsal osteochondromatosis (DCO). Only three families affected by DCO have been reported so far in the literature. We report a fourth family: a 10-year-old girl, her father, and his cousin. Unlike the other reported cases of DCO this family had no carpal or upper limb epiphyseal osteochondromas and many of the other reported associations. The only consistent associated finding in our cases was the presence of multiple parosteal osteochondromatous proliferations. The findings of our cases are, therefore, unique in many ways. These cases may represent a variant of dominant carpotarsal osteochondromatosis or may represent a new entity.
引用
收藏
页码:67 / 70
页数:4
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