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遗传性短指(趾)症的分类与鉴定

Classification and identification of inherited brachydactylies.

作者信息

Fitch N

出版信息

J Med Genet. 1979 Feb;16(1):36-44. doi: 10.1136/jmg.16.1.36.

Abstract

A search for patterns of malformation in the brachydactylies has resulted in new ways to identify the different types. Type A-1 can be characterised by a proportionate reduction of the middle phalanges. Type B is thought to be an amputation-like defect. In type C the fourth middle phalanx is usually the longest, and type E (Riccardi and Holmes, 1974) is characterised by short metacarpals and short distal phalanges. Short stature is usually present in type A-1 and type E brachydactyly (Riccardi and Holmes, 1974) and it may be present in some individuals with brachydactyly C. As short children have short hands, it is possible that in patients with very mild expressions of brachydactyly the cause of the short stature may be overlooked. It is suggested that in every child with proportionate short stature the hands should be carefully examined. If the hands are disproportionately short, if any distal creases are missing, if there is a shortening, however mild, of any finger, if any metacarpals are short, then it is important to have ϰ-rays to look for brachydactyly A-1, C, or E. Much information is still needed. It is important in future reports to have skeletal surveys, pattern profile analyses, and to note the height of children with brachydactyly C. Most interesting of all will be when fetal limbs of each type become available for study.

摘要

对短指畸形的畸形模式进行研究,产生了识别不同类型的新方法。A-1型的特征是中节指骨成比例缩短。B型被认为是类似截肢的缺陷。C型中,第四中节指骨通常最长,而E型(里卡尔迪和霍姆斯,1974年)的特征是掌骨短和远节指骨短。A-1型和E型短指畸形患者通常身材矮小(里卡尔迪和霍姆斯,1974年),C型短指畸形的一些个体也可能身材矮小。由于儿童身材矮小则手也短,因此对于短指畸形表现非常轻微的患者,身材矮小的原因可能会被忽视。建议对每一个身材成比例矮小的儿童都要仔细检查手部。如果手不成比例地短、缺少任何远端褶皱、任何手指有缩短(无论多么轻微)、任何掌骨短,那么进行X线检查以寻找A-1型、C型或E型短指畸形就很重要。仍需要大量信息。在未来的报告中,进行骨骼检查、模式轮廓分析并记录C型短指畸形儿童的身高很重要。最有趣的是每种类型的胎儿肢体何时可用于研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86b0/1012778/a1e531497921/jmedgene00290-0041-a.jpg

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