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无手足畸形的遗传学(“巴西的无手无足家族”):X. 放射学研究

Genetics of acheiropodia ("The handless and footless families of Brazil"): X. Roentgenologic study.

作者信息

Freire-Maia A, Laredo-Filho J, Freire-Maia N

出版信息

Am J Med Genet. 1978;2(4):321-30. doi: 10.1002/ajmg.1320020402.

Abstract

The main radiologic findings from four unrelated cases and two sibs with acheiropodia are presented and discussed. On the basis of such analysis, a clinical and radiologic description of the anomaly is given. The presence of one or more fingers and of a small bone (Bohomoletz bone) in the upper stumps is discussed. These unusual findings in bone structure were assumed to be due to a variability in the expression of the acheiropodia gene. Radiologic studies of some of the acheiropods' normal parents failed to reveal even mild manifestations of the gene in the heterozygous state. No recognizable pattern was found in the dermal ridges on the end of the acheiropods' upper or lower stumps.

摘要

本文呈现并讨论了4例非亲缘关系病例以及2例手足无指畸形同胞的主要放射学检查结果。基于上述分析,给出了该畸形的临床及放射学描述。讨论了上肢残端中一个或多个手指以及一块小骨(博霍莫列茨骨)的存在情况。这些骨骼结构中的异常发现被认为是由于手足无指畸形基因表达的变异性所致。对一些手足无指畸形者正常父母的放射学研究未能发现该基因杂合状态下的哪怕轻微表现。在手无指畸形者上肢或下肢残端末端的皮嵴中未发现可识别的模式。

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