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Klinefelter syndrome and other sex chromosomal aneuploidies

机译:Klinefelter综合征和其他性染色体非整倍性

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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.
机译:术语Klinefelter综合征(KS)描述了一组染色体疾病,其中正常男性核型46,XY至少有一个额外的X染色体。 XXY非整倍性是人类最常见的性染色体疾病,患病率每500名男性中就有1名。也已经描述了其他性染色体非整倍性,尽管它们的频率要低得多,每17,000名男性中有18,000名中有48,XXYY和48,XXXY名男性中有10,000名。 49,XXXXY的发生率是每85,000到100,000个男性出生中就有1个。此外,还存在46,XX例男性,这是由父系减数分裂过程中包括性别决定区(SRY)的Y物质向X染色体的易位引起的。要进行明确的诊断,必须进行正式的细胞遗传学分析,而且生理特征上更明显的差异往往与性染色体数目的增加有关。如果不是产前诊断,则47,XXY位男性可能会出现与年龄有关的各种细微的临床体征。在婴儿期,患有47,XXY的男性可能对尿道下裂,小阴茎或隐睾症,发育迟缓做了染色体评估。学龄儿童可能会出现语言延迟,学习障碍或行为问题。内分泌评估期间可能发现较大的儿童或青少年,因为青春期发育迟缓或不完全,伴有太监样的身体习性,女性乳房发育和小睾丸。通常对成年人进行不育或乳腺恶性肿瘤评估。雄激素替代疗法应在青春期开始,大约在12岁左右,增加剂量以维持年龄,适当的睾丸激素,雌二醇,促卵泡激素(FSH)和促黄体生成激素(LH)的血清浓度。额外X的数量对身体和认知发展的影响增加,每个额外X的智商(IQ)降低约15–16点,其中语言受影响最大,特别是表达语言技能。

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