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男孩克兰费尔特综合征的临床细胞遗传学和精神神经学方面(作者译)

[Clinical cytogenetic and psychoneurological aspects of Klinefelter's syndrome in boys (author's transl)].

作者信息

Szczepski O, Goncerzewicz M, Krawczyński M, Bartkowiak K

出版信息

Monatsschr Kinderheilkd (1902). 1980 Feb;128(2):84-8.

PMID:7189012
Abstract

Investigations were carried out on boys aged between 8 and 20 years by positive chromatin test. Klinefelter's syndrome was confirmed by karyotype determination in 13 cases. In comparison with the average Polish population the patients' parents were older. The patients were usually the last children to be born in their families. Typical hypogonadism, cryptorchism, especially unilateral, and delay in the development of secondary sex characteristics were observed. Besides typical eunuchoid habitus, endomorphic type of body build, tendency towards obesity or sometimes even delay in growth and a deficiency in body weight were noticed. True gynaecomastia was only present in 1/4 of these patients. Very frequent features of Klinefelter's syndrome are--in the authors' opinion--mental subnormality, inadequate social adaptation and neurotic symptoms. Before adolescence the characteristic phenotype of Klinefelter's syndrome is absent. These results indicate that sex chromatin examination is a general screening test to determine Klinefelter's syndrome in boys.

摘要

通过阳性染色质试验对8至20岁的男孩进行了调查。通过核型测定确诊了13例克兰费尔特综合征。与波兰普通人群相比,患者的父母年龄较大。患者通常是其家庭中最后出生的孩子。观察到典型的性腺功能减退、隐睾症,尤其是单侧隐睾症,以及第二性征发育延迟。除了典型的类无睾体型、内胚层体型、肥胖倾向,有时甚至生长发育迟缓及体重不足外,真正的男性乳房发育仅见于1/4的这些患者。作者认为,克兰费尔特综合征非常常见的特征是智力低下、社会适应不良和神经症状。青春期前不存在克兰费尔特综合征的特征性表型。这些结果表明,性染色质检查是确定男孩克兰费尔特综合征的一项常规筛查试验。

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