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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：
LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA MEDICAL CENTER
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
来源：
https://reporter.nih.gov/project-details/6306684
关键词：
Klinefelter's syndrome Turner's syndrome chromosome disorders clinical research cognition disorders dyslexia human subject hypogonadism sex chromosomes

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中文摘要
翻译
目的：研究Klinefelter综合征、等染色体X及其他X、Y染色体遗传性先天性疾病，并调查这些患者的阅读障碍及行为和学习障碍的程度。[目的]探讨携带XXY、XYY、XXX和等位染色体X的Turner综合征患者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、正常性别和年龄组的对照组以及核型相同但阅读障碍特征很少或不存在的受试者进行比较。
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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