A case report on Klinefelter syndrome.

dc.contributor.authorIslam, M Aen_US
dc.contributor.authorRahman, Sen_US
dc.contributor.authorSiddiqui, N Ien_US
dc.contributor.authorSarker, C Ben_US
dc.contributor.authorHossain, Jen_US
dc.contributor.authorHaque, M Aen_US
dc.date.accessioned2004-07-31en_US
dc.date.accessioned2009-05-27T03:53:10Z
dc.date.available2004-07-31en_US
dc.date.available2009-05-27T03:53:10Z
dc.date.issued2004-07-31en_US
dc.descriptionMymensingh Medical Journal.en_US
dc.description.abstractAn 18 year old boy presented with small genitalia, failure of eruption of secondary sex hairs, female like voice with eunachoid body habitus, bilateral gynecomastia, infantile external genitalia, small testes and poorly developed musculature. He was diagnosed as a case of 47XXY Klinefelter syndrome on the basis of hormone assay and karyotyping. He has given androgen replacement therapy with the aim to relieve symptoms of androgen deficiency, to reproduce physiological levels of plasma testosterone and to prevent long term consequences of androgen deficiency.en_US
dc.description.affiliationMymensingh Medical College Hospital, Mymensingh.en_US
dc.identifier.citationIslam MA, Rahman S, Siddiqui NI, Sarker CB, Hossain J, Haque MA. A case report on Klinefelter syndrome. Mymensingh Medical Journal. 2004 Jul; 13(2): 188-90en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/1302
dc.language.isoengen_US
dc.subject.meshAdolescenten_US
dc.subject.meshHumansen_US
dc.subject.meshKlinefelter Syndrome --complicationsen_US
dc.subject.meshMaleen_US
dc.titleA case report on Klinefelter syndrome.en_US
dc.typeCase Reportsen_US
dc.typeJournal Articleen_US
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