Publication:
De Novo Balanced (X;14) Translocation in a Patient With Recurrent Miscarriages: Case Report

dc.authorscopusid56602651500
dc.authorscopusid18038193800
dc.authorscopusid7005424336
dc.authorscopusid6603455076
dc.authorscopusid6603432100
dc.authorscopusid21134879300
dc.contributor.authorAlpaslan Pinarli, F.
dc.contributor.authorÖkten, G.
dc.contributor.authorOzcelik, T.
dc.contributor.authorKara, N.
dc.contributor.authorGüneş, S.
dc.contributor.authorKoçak, I.
dc.date.accessioned2020-06-21T14:39:59Z
dc.date.available2020-06-21T14:39:59Z
dc.date.issued2011
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Alpaslan Pinarli] Ferda, Department of Medical Biology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Ökten] Gülsen, Department of Medical Biology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Ozcelik] Tayfun, Department of Molecular Biology and Genetics, Bilkent Üniversitesi, Ankara, Ankara, Turkey; [Kara] Nurten, Department of Medical Biology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Güneş] Sezgin Özgür, Department of Medical Biology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Koçak] Idris, Gynecology and Obstetrics Department, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_US
dc.description.abstractWe report a 23-year-old phenotypically normal female patient who had previously suffered from recurrent spontaneous abortion (RSA) who found to have an X;14 trans location and a Methylene- Tetrahdrofolate-Reductase (MTHFR) C677T heterozygote mutation. G-banding cytogenetic analysis was cultured from the peripheral blood lymphocy tes. MTHFR, factor V Leiden and prothrombin gene mutations were studied from DNA obtained from peripheral blood lym- phocytes with stripassay. DNA for X inactivation pattern study was also obtained with the method described above. G-banding cytogentic analysis from cultured peripheral blood lymphocytes of the patient revealed 46,XderX,t(X;14)(q13;q32) and found to be heterozygous for C677T MTHFR mutation. An X inactivation pattern study revealed a complete inactivated nor mal X chromosome, asexpected. The possible causes of recurrent miscarriages in our patient were unbalanced gametes, skewed X inactivation and MTHFR C677T heterozygote mutation. © 2011 by Türkiye Klinikleri.en_US
dc.identifier.doi10.5336/medsci.2009-13428
dc.identifier.endpage715en_US
dc.identifier.issn1300-0292
dc.identifier.issue3en_US
dc.identifier.scopus2-s2.0-80051764101
dc.identifier.scopusqualityQ4
dc.identifier.startpage712en_US
dc.identifier.urihttps://doi.org/10.5336/medsci.2009-13428
dc.identifier.volume31en_US
dc.identifier.wosWOS:000293108900029
dc.language.isoenen_US
dc.publisherTurkiye Kliniklerien_US
dc.relation.ispartofTurkiye Klinikleri Journal of Medical Sciencesen_US
dc.relation.journalTurkiye Klinikleri Tip Bilimleri Dergisien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAbortionen_US
dc.subjectGeneticen_US
dc.subjectHabitualen_US
dc.subjectHeterozygote Detectionen_US
dc.subjectTranslocationen_US
dc.subjectX Chromosome Inactivationen_US
dc.titleDe Novo Balanced (X;14) Translocation in a Patient With Recurrent Miscarriages: Case Reporten_US
dc.title.alternativeTekrarlayan Düşükler Yapan Bir Hastada Doğumsal Dengeli (X;14) Translokasyonuen_US
dc.typeArticleen_US
dspace.entity.typePublication

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