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dc.contributor.authorPolat, A
dc.contributor.authorYucel, B
dc.date.accessioned2021-03-05T15:25:38Z
dc.date.available2021-03-05T15:25:38Z
dc.date.issued2003
dc.identifier.citationYucel B., Polat A., "A late sex reassignment in 5-alpha reductase deficiency: Case report", INTERNATIONAL JOURNAL OF PSYCHIATRY IN MEDICINE, cilt.33, ss.189-193, 2003
dc.identifier.issn0091-2174
dc.identifier.othervv_1032021
dc.identifier.otherav_bbd48524-7d9a-434d-a776-59e54fc1c20c
dc.identifier.urihttp://hdl.handle.net/20.500.12627/124870
dc.identifier.urihttps://doi.org/10.2190/2htd-a24d-9k0m-0x4l
dc.description.abstractThe syndrome of male pseudohermaphroditism, caused by a deficiency of the enzyme 5-alpha reductase, results in a selective decrease in dihyrotestosterone. Culture is an important part of the context in which decisions are made on sex assignment of patients with abnormalities of the external genitalia. In Turkey, patients with ambiguious genitalia are diagnosed very late and corrective surgery is usually performed during or after puberty. Here we present a case with 5-alpha reductase deficiency who was diagnosed at puberty and followed-up for 10 years.
dc.language.isoeng
dc.subjectPsikiyatri
dc.subjectSağlık Bilimleri
dc.subjectKlinik Tıp (MED)
dc.titleA late sex reassignment in 5-alpha reductase deficiency: Case report
dc.typeMakale
dc.relation.journalINTERNATIONAL JOURNAL OF PSYCHIATRY IN MEDICINE
dc.contributor.department, ,
dc.identifier.volume33
dc.identifier.issue2
dc.identifier.startpage189
dc.identifier.endpage193
dc.contributor.firstauthorID167195


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