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Dyslexia in 47,XXY boys identified at birth.

作者信息

Bender B G, Puck M H, Salbenblatt J A, Robinson A

出版信息

Behav Genet. 1986 May;16(3):343-54. doi: 10.1007/BF01071315.

DOI:10.1007/BF01071315
PMID:3753369
Abstract
摘要

相似文献

1
Dyslexia in 47,XXY boys identified at birth.出生时确诊的47，XXY男孩的阅读障碍。
Behav Genet. 1986 May;16(3):343-54. doi: 10.1007/BF01071315.
2
Oral and written language abilities of XXY boys: implications for anticipatory guidance.XXY男孩的口语和书面语言能力：对预期指导的启示
Pediatrics. 1988 Jun;81(6):795-806.
3
Expanding the phenotypic profile of boys with 47, XXY: the impact of familial learning disabilities.扩大 47, XXY 男孩表型谱：家族性学习障碍的影响。
Am J Med Genet A. 2014 Jun;164A(6):1464-9. doi: 10.1002/ajmg.a.36483. Epub 2014 Apr 8.
4
Clinical observations in Klinefelter (47,XXY) syndrome.克兰费尔特（47,XXY）综合征的临床观察
J Ment Defic Res. 1978 Sep;22(3):207-12. doi: 10.1111/j.1365-2788.1978.tb00977.x.
5
Predicting intellectual functioning in 47,XXY boys from characteristics of sibs.根据同胞特征预测47，XXY男孩的智力功能。
Clin Genet. 1987 Jul;32(1):24-7. doi: 10.1111/j.1399-0004.1987.tb03318.x.
6
Hormonal replacement therapy and its potential influence on working memory and competency/adaptive functioning in 47,XXY (Klinefelter syndrome).47,XXY（克氏综合征）患者接受激素替代疗法及其对工作记忆和能力/适应功能的潜在影响。
Am J Med Genet A. 2019 Dec;179(12):2374-2381. doi: 10.1002/ajmg.a.61360. Epub 2019 Oct 2.
7
Dyslexia after left occipitotemporal lobectomy: a case report.左枕颞叶切除术后的阅读障碍：一例报告
Cortex. 1973 Sep;9(3):321-8. doi: 10.1016/s0010-9452(73)80010-3.
8
Mental development in polysomy X Klinefelter syndrome (47,XXY; 48,XXXY): effects of incomplete X inactivation.X染色体多体克氏综合征（47,XXY；48,XXXY）的智力发育：X染色体不完全失活的影响
Semin Reprod Med. 2001 Jun;19(2):193-202. doi: 10.1055/s-2001-15400.
9
Cognitive and behavioral factors in the learning disabilities of 47,XXY and 47,XYY boys.47,XXY和47,XYY男孩学习障碍中的认知与行为因素
Birth Defects Orig Artic Ser. 1990;26(4):45-58.
10
What it is said versus how it is said: comprehension of affective prosody in men with Klinefelter (47,XXY) syndrome.所说内容与表达方式：克兰费尔特综合征（47,XXY）男性对情感韵律的理解
J Int Neuropsychol Soc. 2007 Nov;13(6):1065-70. doi: 10.1017/S1355617707071044.

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DNA hypomethylation at specific CG-sites within TRAK1 is linked to the neurocognitive profile in Klinefelter syndrome.TRAK1基因内特定CG位点的DNA低甲基化与克兰费尔特综合征的神经认知特征相关。
Mol Psychiatry. 2025 Sep 30. doi: 10.1038/s41380-025-03254-z.
2
Understanding the Neuropsychological Implications of Klinefelter Syndrome in Pediatric Populations: Current Perspectives.了解克氏综合征在儿科人群中的神经心理学影响：当前观点
Pediatr Rep. 2024 May 25;16(2):420-431. doi: 10.3390/pediatric16020036.
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Supporting students with sex chromosome aneuploidies in educational settings: Results of a nationwide survey.

本文引用的文献

1
TWO CYTOGENETIC SYNDROMES: PSYCHOLOGIC COMPARISONS. I. INTELLIGENCE AND SPECIFIC-FACTOR QUOTIENTS.两种细胞遗传学综合征：心理学比较。I. 智力与特殊因素商数。
J Psychiatr Res. 1964 Oct;2:223-31. doi: 10.1016/0022-3956(64)90022-6.
2
The token test: A sensitive test to detect receptive disturbances in aphasics.令牌测试：一种用于检测失语症患者接受性障碍的敏感测试。
Brain. 1962 Dec;85:665-78. doi: 10.1093/brain/85.4.665.
3
Psychopathology of Klinefelter's syndrome; review of thirty-one cases.
支持性染色体非整倍体学生在教育环境中的发展：全国性调查的结果。
J Sch Psychol. 2022 Aug;93:28-40. doi: 10.1016/j.jsp.2022.06.002. Epub 2022 Jun 28.
4
Executive function in XXY: Comparison of performance-based measures and rating scales.XXY 个体的执行功能：基于表现的测量方法与评定量表的比较。
Am J Med Genet C Semin Med Genet. 2020 Jun;184(2):469-481. doi: 10.1002/ajmg.c.31804. Epub 2020 Jun 9.
5
Early neurodevelopmental and medical profile in children with sex chromosome trisomies: Background for the prospective eXtraordinarY babies study to identify early risk factors and targets for intervention.性染色体三体患儿的早期神经发育和医学特征：开展前瞻性 eXtraordinarY babies 研究以识别早期风险因素和干预靶点的背景。
Am J Med Genet C Semin Med Genet. 2020 Jun;184(2):428-443. doi: 10.1002/ajmg.c.31807. Epub 2020 Jun 7.
6
The Association of Motor Skills and Adaptive Functioning in XXY/Klinefelter and XXYY Syndromes.XXY/Klinefelter 和 XXYY 综合征患者运动技能与适应功能的相关性。
Phys Occup Ther Pediatr. 2019;39(4):446-459. doi: 10.1080/01942638.2018.1541040. Epub 2018 Dec 28.
7
Klinefelter syndrome has increased brain responses to auditory stimuli and motor output, but not to visual stimuli or Stroop adaptation.克兰费尔特综合征患者对听觉刺激和运动输出的大脑反应增强，但对视觉刺激或斯特鲁普适应的反应则不然。
Neuroimage Clin. 2016 Feb 11;11:239-251. doi: 10.1016/j.nicl.2016.02.002. eCollection 2016.
8
Influence of the X-chromosome on neuroanatomy: evidence from Turner and Klinefelter syndromes.X 染色体对神经解剖结构的影响：特纳综合征和克氏综合征的证据。
J Neurosci. 2014 Mar 5;34(10):3509-16. doi: 10.1523/JNEUROSCI.2790-13.2014.
9
Timing of diagnosis of 47,XXY and 48,XXYY: a survey of parent experiences.47,XXY 和 48,XXYY 患者的诊断时间：家长经验调查。
Am J Med Genet A. 2013 Feb;161A(2):268-72. doi: 10.1002/ajmg.a.35709. Epub 2013 Jan 15.
10
Executive function in young males with Klinefelter (XXY) syndrome with and without comorbid attention-deficit/hyperactivity disorder.患有和未患有共病注意缺陷多动障碍的克氏综合征（XXY）年轻男性的执行功能
J Int Neuropsychol Soc. 2011 May;17(3):522-30. doi: 10.1017/S1355617711000312.
Lancet. 1957 Jul 27;273(6987):164-7. doi: 10.1016/s0140-6736(57)90616-5.
4
Learning disorders and sex chromosome aberrations.学习障碍与性染色体畸变
J Ment Defic Res. 1980 Mar;24(1):17-26. doi: 10.1111/j.1365-2788.1980.tb00053.x.
5
Sex chromosomal abnormalities (SCA): a prospective and longitudinal study of newborns identified in an unbiased manner.性染色体异常（SCA）：一项对以无偏倚方式识别出的新生儿进行的前瞻性纵向研究。
Birth Defects Orig Artic Ser. 1982;18(4):7-39.
6
How many kinds of reading disability are there?阅读障碍有多少种类型？
J Learn Disabil. 1982 Oct;15(8):456-60. doi: 10.1177/002221948201500802.
7
Learning disabilities in children with sex chromosome anomalies.性染色体异常儿童的学习障碍
Child Dev. 1982 Oct;53(5):1182-92.
8
Klinefelter's syndrome in adolescence.青春期克氏综合征
Arch Dis Child. 1982 Jan;57(1):6-12.
9
Cognitive profiles in reading disability.阅读障碍中的认知特征。
Genet Psychol Monogr. 1982 Feb;105(First Half):41-93.
10
Speech and language development in 41 children with sex chromosome anomalies.41例性染色体异常儿童的言语和语言发育情况
Pediatrics. 1983 Feb;71(2):262-7.