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克兰费尔特综合征:历史背景与发展

Klinefelter's syndrome: historical background and development.

作者信息

Klinefelter H F

出版信息

South Med J. 1986 Sep;79(9):1089-93.

PMID:3529433
Abstract

When described more than 40 years ago, Klinefelter's syndrome (small testes, sterility, increased excretion of follicle-stimulating hormone, and usually gynecomastia) was thought to be an endocrine disorder. A second testicular hormone was postulated but has never been isolated. During the ensuing years, the syndrome has been found to be a chromosomal disorder, in which there is an extra X chromosome in 80% of the patients. The disorder occurs once in 500 to 1,000 male births and is best diagnosed by a buccal smear. When there is androgen deficiency, it is treated with testosterone. Gynecomastia is treated surgically because of the potential danger of malignancy or for cosmetic reasons.

摘要

40多年前首次描述的克兰费尔特综合征(睾丸小、不育、促卵泡激素排泄增加,通常伴有男性乳房发育)被认为是一种内分泌疾病。当时推测存在第二种睾丸激素,但从未分离出来。在随后的几年里,该综合征被发现是一种染色体疾病,80%的患者存在一条额外的X染色体。这种疾病在每500至1000例男性出生中出现1例,通过口腔黏膜涂片检查最易诊断。出现雄激素缺乏时,用睾酮治疗。由于存在恶变风险或出于美容原因,男性乳房发育需进行手术治疗。

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