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XYY 综合征中的自闭症谱系障碍:两例新病例及文献系统回顾。

Autism spectrum disorders in XYY syndrome: two new cases and systematic review of the literature.

机构信息

Unit of Child Neuropsychiatry, Department of Basic Medical Sciences, Neuroscience and Sense Organs, "Aldo Moro" University of Bari, Bari, Italy,

出版信息

Eur J Pediatr. 2014 Mar;173(3):277-83. doi: 10.1007/s00431-014-2267-9. Epub 2014 Jan 25.

DOI:10.1007/s00431-014-2267-9
PMID:24464091
Abstract

UNLABELLED

Abnormalities of the sex chromosomes (47, XXY, 47 XYY, 45,X/46,XY mosaicism) are frequently associated with Autism Spectrum Disorders (ASD), but the male predisposition to these disorders has not been clearly explained. Previously, the role of the X chromosome was considered important in the ASD mainly because autistic symptoms were detected in genetic syndromes involving X chromosome (fragile X syndrome, Rett syndrome, Klinefelter syndrome). Instead, few studies have analyzed the possible role of the Y chromosome in the ASD. This study explores the role of the Y chromosome in ASD through a systematic literature review about the association between ASD and XYY syndrome and a description of two new cases with this association. The literature review considered studies published in peer-reviewed journals, included in the MEDLINE and PubMed databases, that examined the association between ASD and XYY syndrome. Few studies reported the occurrence of ASD in children with XYY karyotype and the majority of them did not reported a well-defined autism diagnostic category associated with an extra Y chromosome, but several clinical conditions that are generically described as language and social impairment.

CONCLUSION

This study underlines the underestimated role of the Y chromosome in ASD, and we postulate that all the ASD associated with the XYY karyotype may presumably fall within mild degree of ASD as in our cases.

摘要

未加标签

性染色体异常(47,XXY、47,XYY、45,X/46,XY 嵌合体)常与自闭症谱系障碍(ASD)相关,但男性易患这些疾病的原因尚未得到明确解释。此前,X 染色体的作用被认为在 ASD 中很重要,主要是因为在涉及 X 染色体的遗传综合征中发现了自闭症症状(脆性 X 综合征、雷特综合征、克莱恩费尔特综合征)。相反,很少有研究分析 Y 染色体在 ASD 中的可能作用。本研究通过系统地回顾关于 ASD 与 XYY 综合征之间关联的文献,以及描述两例具有这种关联的新病例,探讨了 Y 染色体在 ASD 中的作用。文献综述考虑了发表在同行评议期刊上的研究,这些研究被纳入 MEDLINE 和 PubMed 数据库,以检查 ASD 与 XYY 综合征之间的关联。很少有研究报告 XYY 核型儿童发生 ASD,而且大多数研究没有报告与额外的 Y 染色体相关的明确的自闭症诊断类别,但有几种临床情况通常被描述为语言和社交障碍。

结论

本研究强调了 Y 染色体在 ASD 中的作用被低估,我们假设所有与 XYY 核型相关的 ASD 可能都属于我们病例中的轻度 ASD。

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本文引用的文献

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Sex chromosomes and the brain: a study of neuroanatomy in XYY syndrome.性染色体与大脑:XYY 综合征的神经解剖学研究。
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Early manifestations in a cohort of children prenatally diagnosed with 47,XYY. Role of multidisciplinary counseling for parental guidance and prevention of aggressive behavior.产前诊断为 47,XYY 的患儿队列中的早期表现。多学科咨询对父母指导和预防攻击性行为的作用。
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Commentary: Unravelling the effects of additional sex chromosomes on cognition and communication--reflections on Lee et al. (2012).
Y 染色体基因拷贝数正常且缺乏自闭症表型的男性,其核型为等臂 Y 染色体且 NLGN4Y 表达缺失。
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J Neurodev Disord. 2018 Oct 22;10(1):30. doi: 10.1186/s11689-018-9248-7.
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Rare 48, XYYY syndrome: case report and review of the literature.罕见的48,XYYY综合征:病例报告及文献综述
Clin Case Rep. 2017 Dec 7;6(1):179-184. doi: 10.1002/ccr3.1311. eCollection 2018 Jan.
6
Duplication of Yq- and proximal Yp-arms with deletion of almost all PAR1 (including SHOX) in a young man with non-obstructive azoospermia, short stature and skeletal defects.一名患有非梗阻性无精子症、身材矮小和骨骼缺陷的年轻男性,其Y染色体长臂和近端短臂重复,几乎所有PAR1(包括SHOX)缺失。
J Appl Genet. 2017 Nov;58(4):481-486. doi: 10.1007/s13353-017-0412-7. Epub 2017 Oct 6.
7
High resolution analysis of rare copy number variants in patients with autism spectrum disorder from Taiwan.台湾自闭症谱系障碍患者罕见拷贝数变异的高分辨率分析。
Sci Rep. 2017 Sep 20;7(1):11919. doi: 10.1038/s41598-017-12081-4.
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评论:解析额外性染色体对认知和交流的影响——对李等人(2012年)研究的思考
J Child Psychol Psychiatry. 2012 Oct;53(10):1082-3. doi: 10.1111/j.1469-7610.2012.02610.x. Epub 2012 Aug 31.
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Socio-economic factors affect mortality in 47,XYY syndrome-A comparison with the background population and Klinefelter syndrome.社会经济因素对 47,XYY 综合征患者死亡率的影响-与背景人群和克莱恩费尔特综合征的比较。
Am J Med Genet A. 2012 Oct;158A(10):2421-9. doi: 10.1002/ajmg.a.35539. Epub 2012 Aug 14.
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Dosage effects of X and Y chromosomes on language and social functioning in children with supernumerary sex chromosome aneuploidies: implications for idiopathic language impairment and autism spectrum disorders.性染色体数目异常患儿的 X 和 Y 染色体对语言和社会功能的剂量效应:对特发性语言障碍和自闭症谱系障碍的影响。
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Social deficits in male children and adolescents with sex chromosome aneuploidy: a comparison of XXY, XYY, and XXYY syndromes.性染色体非整倍体男性儿童和青少年的社交缺陷:XXY、XYY 和 XXYY 综合征的比较。
Res Dev Disabil. 2012 Jul-Aug;33(4):1254-63. doi: 10.1016/j.ridd.2012.02.013. Epub 2012 Mar 23.
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Behavioral and social phenotypes in boys with 47,XYY syndrome or 47,XXY Klinefelter syndrome.47,XYY 综合征或 47,XXY 克氏综合征男孩的行为和社会表型。
Pediatrics. 2012 Apr;129(4):769-78. doi: 10.1542/peds.2011-0719. Epub 2012 Mar 12.
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Criminality in men with Klinefelter's syndrome and XYY syndrome: a cohort study.克兰费尔特综合征和XYY综合征男性的犯罪行为:一项队列研究。
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Klinefelter syndrome as a window on the aetiology of language and communication impairments in children: the neuroligin-neurexin hypothesis.克莱恩费尔特综合征:儿童语言和沟通障碍病因研究的窗口——神经黏连蛋白-神经递质假说
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