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38_1277.pdf | 4.76 MB | Adobe PDF | 見る/開く |
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DCフィールド | 値 | 言語 |
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dc.contributor.author | 多田, 実 | ja |
dc.contributor.author | 甲田, 直也 | ja |
dc.contributor.author | 滝本, 至得 | ja |
dc.contributor.alternative | Tada, Minoru | en |
dc.contributor.alternative | Koda, Naoya | en |
dc.contributor.alternative | Takimoto, Yukie | en |
dc.date.accessioned | 2010-06-01T02:57:11Z | - |
dc.date.available | 2010-06-01T02:57:11Z | - |
dc.date.issued | 1992-11 | - |
dc.identifier.issn | 0018-1994 | - |
dc.identifier.uri | http://hdl.handle.net/2433/117698 | - |
dc.description.abstract | The patient was a male child 6 years and 6 months old. He visited our hospital because of bilateral cryptorchism and true phimosis. Since he was found to have fairly small testis, micropenis, and anosmia, endocrinological examination was performed. The plasma levels of luteinizing hormone (LH) and follicle stimulating hormone (FSH) were at the lower limit of normal values. LH gave a low reaction to the LH-releasing hormone test, while the reaction of FSH was near the lower limit of normal values. In the human chorionic gonadotropin test, there was no rise in the plasma levels of testosterone. Nor was there any reaction to the venous olfactory test with Alinamine (thiamine propyldisulfide). Accordingly, the patient was diagnosed as having Kallmann's syndrome. A search of the literature reveals few reports that deal with Kallmann's syndrome in infancy. Early diagnosis seems to be of significance, however, to institute early appropriate treatment to prompt the development of proper secondary sexual characteristics and ensure normal future fertility. | en |
dc.format.mimetype | application/pdf | - |
dc.language.iso | jpn | - |
dc.publisher | 泌尿器科紀要刊行会 | ja |
dc.subject | Kallmann's syndrome | en |
dc.subject | Anosmia | en |
dc.subject | Hypogonodotrophic hypogonadism | en |
dc.subject | Micropenis | en |
dc.subject | Undescended testis | en |
dc.subject.ndc | 494.9 | - |
dc.title | Kallmann症候群の1男児例 | ja |
dc.title.alternative | Kallmann's syndrome in a child--a case report | en |
dc.type | departmental bulletin paper | - |
dc.type.niitype | Departmental Bulletin Paper | - |
dc.identifier.ncid | AN00208315 | - |
dc.identifier.jtitle | 泌尿器科紀要 | ja |
dc.identifier.volume | 38 | - |
dc.identifier.issue | 11 | - |
dc.identifier.spage | 1277 | - |
dc.identifier.epage | 1279 | - |
dc.textversion | publisher | - |
dc.sortkey | 14 | - |
dc.address | 埼玉県立小児医療センター泌尿器科 | ja |
dc.address | 埼玉県立小児医療センター代謝, 内分泌科 | ja |
dc.address | 日本大学駿河台病院泌尿器科 | ja |
dc.address.alternative | the Department of Urology, Saitama Childrens Medical Center | en |
dc.address.alternative | the Division of Metabolismand Endocrinology, Saitama Childrens Medical Center | en |
dc.address.alternative | the Department of Urology, Nihon University Surugadai Hospital | en |
dc.identifier.pmid | 1485582 | - |
dcterms.accessRights | open access | - |
dc.identifier.pissn | 0018-1994 | - |
dc.identifier.jtitle-alternative | Acta urologica Japonica | la |
dc.identifier.jtitle-alternative | Hinyokika Kiyo | en |
出現コレクション: | Vol.38 No.11 |
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