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Two turner syndrome patients with the mosaic 45,X/46,X,i(Xq) karyotype: Case report

dc.contributor.authorGunes, Sezgin
dc.contributor.authorKara, Nurten
dc.contributor.authorSurucu, Bulent
dc.contributor.authorOkten, Gulsen
dc.contributor.authorYigit, Serbuelent
dc.contributor.authorSezer, Ozlem
dc.date.accessioned2020-06-21T15:14:31Z
dc.date.available2020-06-21T15:14:31Z
dc.date.issued2008
dc.identifier.issn1300-0292
dc.identifier.issn2146-9040
dc.identifier.urihttps://hdl.handle.net/20.500.12712/19410
dc.descriptionSEZER, OZLEM/0000-0001-5727-7965en_US
dc.descriptionWOS: 000256246600020en_US
dc.description.abstractTurner's syndrome is one of the most common chromosomal aneuploidy disorders. Turner's syndrome occurs in 1 in 4000 live-born girls and approximately 5 to 10 percent of them have mosaic isochromosome 45,X/46,X,i(Xq). Turner's syndrome is associated with reduced adult height and with gonadal dysgenesis, leading to insufficient circulating levels of female sex steroids and to infertility. In this study, we presented 18 year-old two girls having complaints of primary amenorrhea with mosaic 46,X,i(X)(qter -> q10en_US
dc.language.isoturen_US
dc.publisherOrtadogu Ad Pres & Publ Coen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectTurner syndromeen_US
dc.subjectisochromosomesen_US
dc.titleTwo turner syndrome patients with the mosaic 45,X/46,X,i(Xq) karyotype: Case reporten_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume28en_US
dc.identifier.issue2en_US
dc.identifier.startpage236en_US
dc.identifier.endpage238en_US
dc.relation.journalTurkiye Klinikleri Tip Bilimleri Dergisien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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