Klinefelter syndrome

Determination of Serum Sex Homones and Free Testosterone in 71 Cases of Klinefelter Syndrome

71例克氏综合征患者血清性激素和游离睾酮检测分析

Studies on autoimmunization of klinefelter syndrome & discuss the machenism of developing for anti-sperm antibody

克氏综合征的自身免疫研究&血清抗精子抗体形成的机理探讨

Klinefelter syndrome is the main type of chromosome abnormality in male infertility .

1例（1.52%）为46，XX男性综合征。结论：染色体异常是男性不育的主要原因之一。

The Analysis of Marriage-and-fertility And Investigation On 16 Klinefelter Syndrome

16例克氏征病人婚育及随访资料分析

The study on clinics and cytogenetics of Klinefelter syndrome

Klinefelter综合征的临床与细胞遗传学分析

In Northeast of China , important genetic factor of azoospermic patients were Klinefelter syndrome and Y chromosome microdeletion .

结论：1.中国东北地区无精子患者致病遗传学因素主要为克氏症和Y染色体微缺失。

Objective To investigate the correlation between testicular volume and sex hormone and the pathogenesis of male sterility in Klinefelter syndrome .

目的探讨克氏综合征睾丸体积大小与性激素的相关性及造成克氏综合征男性不育的发病机理。

21 GRAMS Brocade Color The Application of Dual-color Fluorescence in situ Hybridization to the Diagnosis of Klinefelter Syndrome

应用双色荧光原位杂交技术检测克氏综合征

The anti-sperm antibody and morphology of testis in klinefelter syndrome were studied by ELISA and biopsy of testes in this paper .

本文用ELISA和组织活检的方法测定了45例克氏综合征患者血清中IgG、IgA和IgM型抗精子抗体的含量，并观察了其睾丸组织学的变化。

Objective To study in the action of SRY gene in the sex differentiation of the patients with klinefelter syndrome , XY female syndrome and Turner syndrome .

目的探讨Klinefelter综合征、46，XY女性性反转综合征和Turner综合征患者是否存在SRY基因，进一步了解SRY基因在性分化中的作用。

It shows that chromosome abnormal karyotype is relevant to reproductive , growth abnormality . Klinefelter syndrome is still the most common chromosomal disease , balanced translocation accounts for largest proportion of autosomal abnormality .

克氏症仍是最常见的染色体疾病，染色体平衡易位核型占常染色体异常核型比例最大。

This type is called obstructive azoospermia . Primary azoospermia can be divided into Sertoli cell-only syndrome ( SCOS ), complete spermatogenic arrest , Klinefelter syndrome , hypospermatogenesis and so on .

原发性无精子症按生精障碍程度不同又可分为唯支持细胞综合症（SertoliCell-onlysyndromeSCOS）、生精细胞发育完全阻滞、Klinefelter综合症、生精功能低下等常见病理类型。

Twenty cases with sex-differentiating abnormality had been proved by analysis of the karyotype of chromosome . Three cases belonged to syndromes of abnormal sex chromosome such as Turner 's syndrome , xyy syndrome and Klinefelter syndrome .

本文性分化异常20例经染色体核型分析证实：性染色体异常综合征3例，含Turner综合征、xyy综合征、xxy综合征；

Objective : To study the clinical characteristics , diagnosis and treatment of Klinefelter s syndrome .

前言：目的：探讨克氏综合征即先天性睾丸发育不全的临床特点及诊治方法。

Clinical genetics studies of 40 patients with klinefelter 's syndrome

40例Klinefelter综合征的临床遗传学研究

The Measurement on Base Value of 9 Serum Hormones in Klinefelter 's Syndrome

Klinefelter's综合征患者9项血清激素基础值的测定

Chromosomal analysis of 85 cases of Klinefelter 's syndrome in Zhanjiang area

湛江地区85例Klinefelter综合征染色体分析

Study on pituitary-gonadal function in patients with klinefelter 's syndrome

Klinefelter氏综合征患者垂体-性腺内分泌功能研究

Klinefelter 's Syndrome ( A Case Report )

Klinefelter氏综合征（附病例报告）

Acute pulmonary thromboembolism associated with Klinefelter 's syndrome : the first case report and review of the literature in china

先天性睾丸发育不全综合征并发肺血栓栓塞症1例并文献复习

X chromosome centromeric alpha satellite DNA variation in Klinefelter 's syndrome patients and their parents

Klinefelter综合征及双亲X染色体着丝粒区α-卫星DNA变异研究

Effect of testosterone undecanoate on the function of pituitary testis axis in the patients with Klinefelter 's syndrome

十一酸睾酮对Klinefelter综合征患者垂体性腺轴系功能的影响

Sexual chromosome abnormalities were most commen , 31 cases of them were Klinefelter 's syndrome ( 15.50 % );

性染色体异常最多，并以克氏征（Klinefelter'sSyndrome）为主，共31例，占全部病例的15.50%。

You have klinefelter 's syndrome .

你有柯林菲特氏症。

Objective : To analysis the aneuploidy rate of X , Y and 18 chromosomes of sperms from a patient of Klinefelter 's syndrome and to guide the assisted reproductive treatment .

目的分析Klinefelter综合征病人精子X，Y，18染色体的非整倍体率（aneuploid），指导其辅助生育治疗。

Patients with Klinefelter 's syndrome are generally characterized by a 47 , XXY karyotype , seminiferous tubule dysgenesis , azoospermia and infertility .

Klinefelter综合征患者以47，XXY核型，睾丸精曲小管发育不良，无精子症和不育为特征。

Objective : To study the variation of X chromosome centromeric Alpha Satellite DNA in Klinefelter 's syndrome patients , their parents and normal individuals and to discuss the mechanism of Klinefelter 's syndrome X chromosome nondisjunction .

目的：本文从DNA分子水平对Klinifelter综合征患者及双亲X染色体着丝粒区域的α-卫星DNA变异进行研究，探讨Klinefelter综合征患者X染色体不分离形成的原因。

Detection of Y chromosome microdeletions in azoospermic patients with Klinefelter ′ s syndrome

Klinefelter综合征Y染色体微缺失的检测