Department of Growth and Reproduction GR, Rigshospitalet, Blegdamsvej, Copenhagen Ø, Denmark.
Am J Med Genet C Semin Med Genet. 2013 Feb 15;163C(1):55-63. doi: 10.1002/ajmg.c.31349. Epub 2013 Jan 23.
47,XXY (Klinefelter syndrome) is the most frequent sex chromosomal disorder and affects approximately one in 660 newborn boys. The syndrome is characterized by varying degrees of cognitive, social, behavioral, and learning difficulties and in adulthood additionally primary testicular failure with small testes, hypergonadotropic hypogonadism, tall stature, and eunuchoid body proportions. The phenotype is variable ranging from "near-normal" to a significantly affected individual. In addition, newborns with Klinefelter syndrome generally present with a normal male phenotype and the only consistent clinical finding in KS is small testes, that are most often not identified until after puberty. Decreased awareness of this syndrome among health professionals and a general perception that all patients with 47,XXY exhibit the classic textbook phenotype results in a highly under-diagnosed condition with up to 75% of the patients left undetected. Typically, diagnosis is delayed with the majority of patients identified during fertility workup in adulthood, and only 10% of patients diagnosed prior to puberty. Early detection of this syndrome is recommended in order to offer treatment and intervention at the appropriate ages and stages of development for the purpose of preventing osteopenia/osteoporosis, metabolic syndrome, and other medical conditions related to hypogonadism and to the XXY as well as minimizing potential learning and psychosocial problems. The aim of this review is to present the clinical aspects of XXY and the age-specific recommendations for medical management. © 2013 Wiley Periodicals, Inc.
47,XXY(克氏综合征)是最常见的性染色体疾病,影响约每 660 名新生男婴中的 1 名。该综合征的特征是认知、社会、行为和学习困难程度不同,成年后还会出现原发性睾丸功能衰竭、睾丸小、促性腺激素性性腺功能减退症、身材高大和男性体型。表型变化范围大,从“接近正常”到明显受影响的个体不等。此外,克氏综合征新生儿通常表现出正常的男性表型,KS 的唯一一致临床发现是睾丸小,这些通常在青春期后才被发现。由于医疗保健专业人员对此综合征的认识不足,以及普遍认为所有 47,XXY 患者都表现出经典教科书表型,导致该疾病的诊断率非常低,高达 75%的患者未被发现。通常,诊断会延迟,大多数患者在成年期进行生育检查时被发现,只有 10%的患者在青春期前被诊断出。建议早期发现该综合征,以便在适当的年龄和发育阶段提供治疗和干预,以预防骨质疏松症/骨质疏松症、代谢综合征和其他与性腺功能减退和 XXY 相关的医疗状况,并最大限度地减少潜在的学习和心理社会问题。本综述的目的是介绍 XXY 的临床方面以及特定年龄段的医学管理建议。