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COGNITIVE DYSFUNCTION IN KLINEFELTERS SYNDROME & OTHER SEX CHROMOSOME DISORDERS

COGNITIVE DYSFUNCTION IN KLINEFELTERS SYNDROME & OTHER SEX CHROMOSOME DISORDERS
克兰费尔特综合征的认知功能障碍
批准号:
6306684
负责人:
RONALD Sherwin SWERDLOFF
金额:
$0.1万
依托单位国家:
美国
项目类别:
财政年份:
1999
资助国家:
美国
项目状态:
已结题
起止时间:
1999-12-01 至 2000-11-30

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项目成果

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中文摘要
翻译
研究克氏综合征、X同染色体及其他X、Y疾病患者的X、Y染色体相关的遗传性先天性疾病,探讨这些患者的阅读障碍、行为和学习障碍的程度。探讨XXY、XYY、XXX和X同染色体特纳氏综合征个体阅读障碍表型的异同。他们将与原发性性腺功能低下的XY男性,正常性别和年龄组对照,以及具有相同核型但很少或没有阅读障碍特征的受试者进行比较。
英文摘要
To study the inherited congenital disorders associated with the X and Y chromosomes in patients with Klinefelter's Syndrome, Isochromosome X, and other X and Y conditions and to investigate to what degree these patients suffer from dyslexia and behavioral and learning disabilities. To identify the similarities/differences in the dyslexic phenotype of individuals with XXY, XYY, XXX and isochromosome X Turner's Syndrome subjects. They will be compared to primary hypogonadal XY men,normal gender and age group controls, and subjects with the same karyotype but with minimal or absent dyslexic features.
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