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X连锁巨睾症与智力迟钝综合征:进一步观察

The X-linked syndrome of macroorchidism and mental retardation: further observations.

作者信息

Bowen P, Biederman B, Swallow K A

出版信息

Am J Med Genet. 1978;2(4):409-14. doi: 10.1002/ajmg.1320020410.

Abstract

We report six males with the syndrome of macroorchidism and mental retardation. The trait is inherited as though X-linked, or possibly autosomal dominant male-limited. We also found no evidence of gonadal dysfunction. Associated abnormalities were abnormal EEG (3/4), seizures (2/6), and one instance each of cervical vertebral fusion, cataract, esophoria, and abnormal cutaneous pigmentation. One woman with a 50% a priori risk of bearing the mutant gene had mental retardation and seizures. Results of Xg blood-group typing were uninformative for the purpose of linkage analysis.

摘要

我们报告了6名患有巨睾症和智力迟钝综合征的男性。该性状的遗传方式似乎是X连锁的,或者可能是常染色体显性限男性遗传。我们也没有发现性腺功能障碍的证据。相关异常包括异常脑电图(3/4)、癫痫发作(2/6),以及各1例颈椎融合、白内障、内斜视和皮肤色素沉着异常。一名携带突变基因的先验风险为50%的女性有智力迟钝和癫痫发作。Xg血型分型结果对连锁分析无帮助。

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