Klinefelter syndrome: The characterization of the clinical and sociological features of 51 patients

IF 0.8 4区 医学 Q4 ANDROLOGY
Fernando Mendonça , Selma Souto , Sofia Dória , Davide Carvalho
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引用次数: 0

Abstract

Introduction

Klinefelter syndrome is the most frequently found aneuploidy among male patients. Its clinical presentation is very heterogeneous, and thus poses a challenge for a timely diagnosis.

Methods

A retrospective study was carried out with 51 consecutively selected patients diagnosed with Klinefelter Syndrome from Jan/2010 to Dec/2019. The karyotypes were identified using high resolution GTL banding at the Genetics Department. Multiple clinical and sociological parameters were studied by collecting data from the clinical records.

Results

44 (86%) of the 51 patients presented a classical karyotype (47,XXY) and 7 (14%) showed evidence of mosaicism. The mean age at diagnosis was 30.2 ± 14.3 years old. Regarding the level of education (N = 44), 26 patients (59.1%) had no secondary education, with 5 (11.4%) patients having concluded university studies. Almost two thirds of the sample revealed learning difficulties (25/38) and some degree of intellectual disability was present in 13.6% (6/44). Half of the patients were either non-qualified workers (19.6%) or workers in industry, construction, and trades (30.4%), which are jobs that characteristically require a low level of education. The proportion of unemployed patients was 6.5%. The main complaints were infertility (54.2%), followed by hypogonadism-related issues (18.7%) and gynecomastia (8.3%). 10 patients (23.8%, N = 42) were biological parents. With regards the question of fertility, assisted reproductive techniques were used in 39.6% of the studied subjects (N = 48), with a success rate (a take home baby) of 57.9% (11/19), 2 with donor sperm and 9 with the patients’ own gametes. Only 41% of the patients (17/41) were treated with testosterone.

Conclusion

This study identifies the most important clinical and sociological findings of Klinefelter syndrome patients that should be considered when deciding workout and disease management.

克氏综合征:51例患者的临床和社会学特征
引言克氏综合征是男性患者中最常见的非整倍体。其临床表现非常异质,因此对及时诊断提出了挑战。方法对2010年1月至2019年12月连续选择的51例克氏综合征患者进行回顾性研究。这些核型是在遗传学部门使用高分辨率GTL条带进行鉴定的。通过从临床记录中收集数据来研究多种临床和社会学参数。结果51例患者中44例(86%)出现典型核型(47,XXY),7例(14%)出现嵌合体。诊断时的平均年龄为30.2±14.3岁。关于教育水平(N=44),26名患者(59.1%)没有受过中等教育,其中5名患者(11.4%)完成了大学研究。近三分之二的样本显示有学习困难(25/38),13.6%(6/44)存在一定程度的智力残疾。一半的患者要么是不合格的工人(19.6%),要么是工业、建筑和行业的工人(30.4%),这些工作通常需要低教育水平。失业患者的比例为6.5%。主要主诉为不孕(54.2%),其次是性腺功能减退相关问题(18.7%)和女性乳房发育症(8.3%)。10名患者(23.8%,N=42)为亲生父母。关于生育问题,39.6%的受试者(N=48)使用了辅助生殖技术,成功率(带回家的婴儿)为57.9%(11/19),2例使用供体精子,9例使用患者自己的配子。只有41%的患者(17/41)接受了睾酮治疗。结论本研究确定了克氏综合征患者最重要的临床和社会学发现,在决定锻炼和疾病管理时应予以考虑。
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来源期刊
CiteScore
1.60
自引率
12.50%
发文量
54
审稿时长
>12 weeks
期刊介绍: Revista Internacional de Andrología es la revista oficial de la Asociación Española de Andrología, Medicina Sexual y Reproductiva (ASESA), la Sociedade Portuguesa de Ardrologia, la Sociedad Argentina de Andrología (SAA), la Asociación Iberoamericana de Sociedades de Andrología (ANDRO), y la Federación Española de Sociedades de Sexología. La revista publicada trimestralmente es revisada por pares y es líder en el la especialidad y en español y portugués. Recientemente también publica artículos en inglés. El objetivo de la revista es principalmente la promoción del conocimiento y la educación médica continua, con un enfoque especial en el público español y latinoamericano, a través de la publicación de las contribuciones importantes de la investigación en el campo. Todos los miembros de las sociedades antes mencionadas reciben la revista y otros suscriptores individuales e institucionales de España, Portugal y América Latina.
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