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阿佩尔综合征中的手部和足部表现。

Hands and feet in the Apert syndrome.

作者信息

Cohen M M, Kreiborg S

机构信息

Department of Oral Biology, Faculty of Dentistry, Dalhousie University, Halifax, Nova Scotia, Canada.

出版信息

Am J Med Genet. 1995 May 22;57(1):82-96. doi: 10.1002/ajmg.1320570119.

DOI:10.1002/ajmg.1320570119
PMID:7645606
Abstract

We studied 44 pairs of hands and 37 pairs of feet in Apert syndrome, utilizing clinical, dermatoglyphic, and radiographic methods. We also studied histologic sections of the hand from a 31-week stillborn fetus. Topic headings discussed include: clinical classification of syndactyly; correlations between types of hands and feet in the same patient; dermatoglyphics; anatomy of the hand; radiologic assessment; comparison with other studies; histologic assessment of the hand; acrocephalosyndactyly vs. acrocephalopolysyndactyly: a pseudodistinction; and some generalizations.

摘要

我们运用临床、皮纹学和放射学方法,对44例Apert综合征患者的手部以及37例患者的足部进行了研究。我们还对一名31周死产胎儿的手部组织切片进行了研究。讨论的主题包括:并指的临床分类;同一患者手部和足部类型之间的相关性;皮纹学;手部解剖;放射学评估;与其他研究的比较;手部组织学评估;尖头并指畸形与尖头多指并指畸形:一种假区别;以及一些概括性内容。

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1
Hands and feet in the Apert syndrome.阿佩尔综合征中的手部和足部表现。
Am J Med Genet. 1995 May 22;57(1):82-96. doi: 10.1002/ajmg.1320570119.
2
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A boy with severe manifestations of type A1 brachydactyly.一名患有A1型短指症严重表现的男孩。
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