Klinefelter综合征,1993年。58例的多中心研究结果及文献综述]。

Annales de pediatrie Pub Date : 1993-09-01
J Battin, G Malpuech, J L Nivelon, P Garandeau, F Freycon, C Sultan, M Bost, G Simonin, J Bouquier, P Rochiccioli
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引用次数: 0

摘要

一项多中心回顾性研究发现58例Klinefelter综合征,其中23例(39%)在青春期前被诊断。虽然与唐氏综合症一样常见,但克氏综合症的诊断不足,通常只有在成年后才会被发现。婴儿、儿童和青少年的暗示性表现包括面部畸形、小阴茎和语言迟缓,应进行核型检查。通过常规测量11 - 15岁学龄男孩的睾丸大小,并对体积小于2ml的男孩进行核型,可以实现克氏综合征的早期识别。在青春期开始时进行早期心理和教育支持以及睾酮替代治疗可能会改善社会和学业成绩。
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[Klinefelter syndrome in 1993. Results of a multicenter study on 58 cases and review of the literature].

A retrospective multicenter study found 58 cases of Klinefelter syndrome of which 23 (39%) were diagnosed before puberty. Although as common as Down syndrome, Klinefelter syndrome is underdiagnosed and often recognized only in adulthood. Suggestive manifestations in infants, children, and teenagers include facial dysmorphism, micropenis, and delayed speech and should lead to examination of the karyotype. Early recognition of Klinefelter syndrome could be achieved by routinely measuring the size of the testes in school-boys aged 11 to 15 years and performing a karyotype in boys with a volume of less than 2 ml. Early psychological and educational support and testosterone replacement therapy initiated at onset of puberty may lead to improved social and academic outcomes.

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