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Titlebook: Klinefelter’s Syndrome; Hans-Jürgen Bandmann,Reinhardt Breit,Elmar Perwein Conference proceedings 1984 Springer-Verlag Berlin Heidelberg 1

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发表于 2025-3-21 17:24:45 | 显示全部楼层 |阅读模式
书目名称Klinefelter’s Syndrome
编辑Hans-Jürgen Bandmann,Reinhardt Breit,Elmar Perwein
视频videohttp://file.papertrans.cn/544/543491/543491.mp4
图书封面Titlebook: Klinefelter’s Syndrome;  Hans-Jürgen Bandmann,Reinhardt Breit,Elmar Perwein Conference proceedings 1984 Springer-Verlag Berlin Heidelberg 1
描述Klinefelter‘s syndrome occurs relatively frequently, being diagnosed for one in 600 male infants, yet it is probably very rare that it is recognized early enough to make effective treatment possible. Often the person afflicted does not go to a doctor until physical and emotional disturbances have developed on the ba­ sis of the syndrome. The appropriate therapy at the correct time can prevent many of these disturbances. In our andrology outpatient clinic we encountered Klinefelter‘s syndrome almost three decades ago in patients suffering from impotentia generandi. It was not until later that we dealt with it in our capacities as dematologists. It was observed at a rate too high to be coincidental among younger men suffer­ ing from ulcera crurum. On the other hand, we failed to see the condition during our work as con­ sultants in other specialities, especially internal medicine, although we re­ peatedly attempted to identify it. We should have encountered it at least occa­ sionally in our 10 years working in the Munich hospitals with their more than 4000 beds. It was this imbalance between the allegedly relative frequency of this condition and its rare detection which led us to pla
出版日期Conference proceedings 1984
关键词Syndrome; child; childhood; histology; hormone; hormones; testis
版次1
doihttps://doi.org/10.1007/978-3-642-69644-2
isbn_softcover978-3-540-13267-7
isbn_ebook978-3-642-69644-2
copyrightSpringer-Verlag Berlin Heidelberg 1984
The information of publication is updating

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发表于 2025-3-21 22:37:00 | 显示全部楼层
Conference proceedings 1984arly enough to make effective treatment possible. Often the person afflicted does not go to a doctor until physical and emotional disturbances have developed on the ba­ sis of the syndrome. The appropriate therapy at the correct time can prevent many of these disturbances. In our andrology outpatien
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,The Clinical Appearance of Klinefelter’s Syndrome,t. Category 1 in fact contains only one symptom, namely small testicular size. Several clinical symptoms belong to category 2, e.g. gynecomastia, skeletal defects, and varicose veins. We have studied the clinical data of 41 patients with KS and present these data below.
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,Klinefelter’s Syndrome and Testicular Tumors,le for this association: (a) chromosomal/genetic, and (b) hormonal/endocrine. Interactions and combinations of these two types of cause may frequently be involved. Immune deficencies may also play a role (Tsung and Heckman 1974).
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,Klinefelter’s Syndrome and Leukemia: Coincidence or Association?,ue in 1970 provided the opportunity not only to recognize the individual human chromosomes but also to demonstrate structural abnormalities. The Philadelphia chromosome, for example, proved to be originated by a translocation between the chromosomes 9 and 22.
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