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与等臂双着丝粒Y染色体相关的孤独症谱系障碍。

Autistic disorder associated with an iso-dicentric Y chromosome.

作者信息

Blackman J A, Selzer S C, Patil S, Van Dyke D C

机构信息

Kluge Children's Rehabilitation Center and Research Institute, University of Virginia, Charlottesville 22901.

出版信息

Dev Med Child Neurol. 1991 Feb;33(2):162-6. doi: 10.1111/j.1469-8749.1991.tb05096.x.

Abstract

The relationship between a fragile site on the X chromosome and autism has been well documented. The authors report a three-year-old child with partial duplication of the short arm of chromosome Y, who had an autistic disorder. He was microcephalic, but otherwise had a normal phenotype. There was a history of preterm birth and maternal diabetes. This is the sixth case of sex chromosome Y aneuploidy associated with autism, but the first with an isodicentric Y. In well-substantiated cases of autism, clinicians should now consider abnormalities of the Y as well as the X chromosome.

摘要

X染色体上的一个脆性位点与自闭症之间的关系已有充分记录。作者报告了一名三岁儿童,其Y染色体短臂部分重复,患有自闭症谱系障碍。他头小畸形,但其他方面具有正常的表型。有早产和母亲患糖尿病的病史。这是第六例与自闭症相关的性染色体Y非整倍体病例,但第一例是等臂双着丝粒Y染色体。在自闭症确诊的病例中,临床医生现在应考虑Y染色体以及X染色体的异常情况。

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