Publication: De Novo Balanced (X;14) Translocation in a Patient With Recurrent Miscarriages: Case Report
| dc.authorscopusid | 56602651500 | |
| dc.authorscopusid | 18038193800 | |
| dc.authorscopusid | 7005424336 | |
| dc.authorscopusid | 6603455076 | |
| dc.authorscopusid | 6603432100 | |
| dc.authorscopusid | 21134879300 | |
| dc.contributor.author | Alpaslan Pinarli, F. | |
| dc.contributor.author | Ökten, G. | |
| dc.contributor.author | Ozcelik, T. | |
| dc.contributor.author | Kara, N. | |
| dc.contributor.author | Güneş, S. | |
| dc.contributor.author | Koçak, I. | |
| dc.date.accessioned | 2020-06-21T14:39:59Z | |
| dc.date.available | 2020-06-21T14:39:59Z | |
| dc.date.issued | 2011 | |
| dc.department | Ondokuz Mayıs Üniversitesi | en_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, Turkey | en_US |
| dc.description.abstract | We 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.doi | 10.5336/medsci.2009-13428 | |
| dc.identifier.endpage | 715 | en_US |
| dc.identifier.issn | 1300-0292 | |
| dc.identifier.issue | 3 | en_US |
| dc.identifier.scopus | 2-s2.0-80051764101 | |
| dc.identifier.scopusquality | Q4 | |
| dc.identifier.startpage | 712 | en_US |
| dc.identifier.uri | https://doi.org/10.5336/medsci.2009-13428 | |
| dc.identifier.volume | 31 | en_US |
| dc.identifier.wos | WOS:000293108900029 | |
| dc.language.iso | en | en_US |
| dc.publisher | Turkiye Klinikleri | en_US |
| dc.relation.ispartof | Turkiye Klinikleri Journal of Medical Sciences | en_US |
| dc.relation.journal | Turkiye Klinikleri Tip Bilimleri Dergisi | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.subject | Abortion | en_US |
| dc.subject | Genetic | en_US |
| dc.subject | Habitual | en_US |
| dc.subject | Heterozygote Detection | en_US |
| dc.subject | Translocation | en_US |
| dc.subject | X Chromosome Inactivation | en_US |
| dc.title | De Novo Balanced (X;14) Translocation in a Patient With Recurrent Miscarriages: Case Report | en_US |
| dc.title.alternative | Tekrarlayan Düşükler Yapan Bir Hastada Doğumsal Dengeli (X;14) Translokasyonu | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication |
