Please use this identifier to cite or link to this item: http://20.193.157.4:9595/xmlui/handle/123456789/4155
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dc.contributor.authorBiradar, Siddanagouda M-
dc.contributor.authorBulagouda, Rudragouda S-
dc.contributor.authorKadakol, Gurushantappa-
dc.date.accessioned2022-02-18T06:25:15Z-
dc.date.available2022-02-18T06:25:15Z-
dc.date.issued2022-
dc.identifier.urihttp://hdl.handle.net/123456789/4155-
dc.description.abstractKlinefelter Syndrome is a chromosomal disorder with addition of X sex chromosome (47XXY) in males. A patient attended to our hospital with loss of secondary sexual characteristics and male infertility. Physical examination revealed thin built, hypogonadism and absence of pubic hairs. Karyotype and biochemical analysis were performed to detect chromosomal abnormality as well as hormonal level to confirm the diagnosis of Klinefelter syndromeen_US
dc.language.isoenen_US
dc.publisherBLDE( Deemed to be University)en_US
dc.subjectKlinefelter Syndrome,en_US
dc.subjectGynecomastiaen_US
dc.titleClinical & Cytological Study on Klinefelter Syndromeen_US
dc.typeArticleen_US
Appears in Collections:Faculty of Anatomy

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