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阿什肯纳兹犹太人中特发性扭转性肌张力障碍的遗传方式

Inheritance of idiopathic torsion dystonia among Ashkenazi Jews.

作者信息

Bressman S B, de Leon D, Brin M F, Risch N, Shale H, Burke R E, Greene P E, Fahn S

机构信息

Department of Neurology, Columbia University College of Physicians and Surgeons, New York, New York 10032.

出版信息

Adv Neurol. 1988;50:45-56.

PMID:3400502
Abstract

The mechanism(s) of inheritance of primary dystonia are unclear. An autosomal recessive form among Ashkenazi Jews and an autosomal dominant form among non-Jews have been proposed. However, the patterns of inheritance, particularly among Ashkenazim, are controversial. In this report we have reviewed the literature particularly as it pertains to the mode of inheritance among Ashkenazim. We also report the results of a pilot study of the families of 25 independently ascertained Ashkenazi probands with onset of primary dystonia before age 27 years. A total of 91/98 living first-degree relatives were examined; of these 91, 86 were greater than or equal to 8 years of age at time of examination and were included in our analysis. Overall, 14/86 (16.3%) of first-degree relatives were affected. We found 11.4% (4/35) of parents, 22.2% (8/36) of siblings, and 13.3% (2/15) of offspring were definitely affected. This finding of an approximately equal risk to parents, siblings, and offspring is consistent with autosomal dominant transmission with a minimum penetrance of 32.6%. Our findings do not support autosomal recessive or multifactorial inheritance.

摘要

原发性肌张力障碍的遗传机制尚不清楚。有人提出在德系犹太人中存在常染色体隐性遗传形式,在非犹太人中存在常染色体显性遗传形式。然而,遗传模式,尤其是在德系犹太人中的遗传模式存在争议。在本报告中,我们回顾了相关文献,特别是与德系犹太人的遗传模式有关的文献。我们还报告了一项针对25名独立确诊的德系犹太先证者的研究结果,这些先证者原发性肌张力障碍发病年龄在27岁之前。总共对91/98名在世的一级亲属进行了检查;其中91人在检查时年龄大于或等于8岁,并纳入我们的分析。总体而言,14/86(16.3%)的一级亲属受影响。我们发现父母中有11.4%(4/35)、兄弟姐妹中有22.2%(8/36)、后代中有13.3%(2/15)受到明确影响。父母、兄弟姐妹和后代的风险大致相等这一发现与常染色体显性遗传一致,最小外显率为32.6%。我们的研究结果不支持常染色体隐性遗传或多因素遗传。

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