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克兰费尔特综合征及其他性染色体非整倍体疾病。

Klinefelter syndrome and other sex chromosomal aneuploidies.

作者信息

Visootsak Jeannie, Graham John M

机构信息

Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30033, USA.

出版信息

Orphanet J Rare Dis. 2006 Oct 24;1:42. doi: 10.1186/1750-1172-1-42.

Abstract

The term Klinefelter syndrome (KS) describes a group of chromosomal disorder in which there is at least one extra X chromosome to a normal male karyotype, 46,XY. XXY aneuploidy is the most common disorder of sex chromosomes in humans, with prevalence of one in 500 males. Other sex chromosomal aneuploidies have also been described, although they are much less frequent, with 48,XXYY and 48,XXXY being present in 1 per 17,000 to 1 per 50,000 male births. The incidence of 49,XXXXY is 1 per 85,000 to 100,000 male births. In addition, 46,XX males also exist and it is caused by translocation of Y material including sex determining region (SRY) to the X chromosome during paternal meiosis. Formal cytogenetic analysis is necessary to make a definite diagnosis, and more obvious differences in physical features tend to be associated with increasing numbers of sex chromosomes. If the diagnosis is not made prenatally, 47,XXY males may present with a variety of subtle clinical signs that are age-related. In infancy, males with 47,XXY may have chromosomal evaluations done for hypospadias, small phallus or cryptorchidism, developmental delay. The school-aged child may present with language delay, learning disabilities, or behavioral problems. The older child or adolescent may be discovered during an endocrine evaluation for delayed or incomplete pubertal development with eunuchoid body habitus, gynecomastia, and small testes. Adults are often evaluated for infertility or breast malignancy. Androgen replacement therapy should begin at puberty, around age 12 years, in increasing dosage sufficient to maintain age appropriate serum concentrations of testosterone, estradiol, follicle stimulating hormone (FSH), and luteinizing hormone (LH). The effects on physical and cognitive development increase with the number of extra Xs, and each extra X is associated with an intelligence quotient (IQ) decrease of approximately 15-16 points, with language most affected, particularly expressive language skills.

摘要

克氏综合征(KS)这一术语描述了一组染色体疾病,其中正常男性核型46,XY中至少多了一条X染色体。XXY非整倍体是人类最常见的性染色体疾病,在男性中的患病率为1/500。其他性染色体非整倍体也有相关描述,不过它们的发生频率要低得多,48,XXYY和48,XXXY在每17000至50000例男性出生中出现1例。49,XXXXY的发病率为每85000至100000例男性出生中出现1例。此外,46,XX男性也存在,它是由父本减数分裂期间Y物质(包括性别决定区域,即SRY)易位到X染色体所致。进行明确诊断需要正式的细胞遗传学分析,身体特征上更明显的差异往往与性染色体数量增加有关。如果在产前未做出诊断,47,XXY男性可能会出现各种与年龄相关的细微临床体征。在婴儿期,47,XXY男性可能因尿道下裂、小阴茎或隐睾症、发育迟缓而进行染色体评估。学龄儿童可能会出现语言发育迟缓、学习障碍或行为问题。年龄较大的儿童或青少年可能在因青春期发育延迟或不完全、具有类无睾体型、乳腺增生和小睾丸而进行内分泌评估时被发现。成年人常因不育或乳腺恶性肿瘤接受评估。雄激素替代疗法应在青春期开始,大约12岁左右,逐渐增加剂量,以维持与年龄相符的血清睾酮、雌二醇、卵泡刺激素(FSH)和黄体生成素(LH)浓度。额外X染色体数量越多,对身体和认知发育的影响就越大,每多一条X染色体,智商(IQ)大约降低15 - 16分,其中语言受影响最大,尤其是表达性语言技能。

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