多重X和Y染色体疾病的社会功能:XXY, XYY, XXYY, XXXY

Jeannie Visootsak, John M. Graham Jr.
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引用次数: 84

摘要

Klinefelter综合征(47,XXY)最初是在其内分泌和生理特征的背景下被描述的;然而,随后的研究揭示了语言技能和社会功能的特殊损害。已知性染色体非整倍体的男性在其发育概况中具有可变性,其中大多数表现为表达性语言缺陷。由于语言发育迟缓,他们更有可能出现语言学习障碍和社交情绪问题,这些问题可能会持续到成年。对患有47,xxy的男性的研究揭示了独特的行为和社会特征,可能易患自闭症。男性多出一条性染色体(如48,xxyy和48,xxxy)和多出一条Y染色体(如47,xyy)的患病率较低,但了解其社会功能很重要,因为它可以深入了解治疗意义。©2009 Wiley-Liss, Inc。发展与残疾,2009;15:28 - 332。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Social function in multiple X and Y chromosome disorders: XXY, XYY, XXYY, XXXY

Klinefelter syndrome (47,XXY) was initially described in the context of its endocrinologic and physical features; however, subsequent studies have revealed specific impairments in verbal skills and social functioning. Males with sex chromosomal aneuploidies are known to have variability in their developmental profile with the majority presenting with expressive language deficits. As a consequence of language delays, they have an increased likelihood of language-based learning disabilities and social-emotional problems that may persist through adulthood. Studies on males with 47,XXY have revealed unique behavioral and social profiles with possible vulnerability to autistic traits. The prevalence of males with more than one extra sex chromosome (e.g., 48,XXYY and 48,XXXY) and an additional Y (e.g., 47,XYY) is less common, but it is important to understand their social functioning as it provides insight into treatment implications. © 2009 Wiley-Liss, Inc. Dev Disabil Res Rev 2009;15:328–332.

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