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dc.contributor.authorDEVRANOGLU, B.
dc.contributor.authorKARAMAN, A.
dc.contributor.authorSAYAR, C.
dc.contributor.authorSÖYLEMEZ, MEHMET ALİ
dc.contributor.authorToksoy, Güven
dc.contributor.authorAYDIN, H.
dc.contributor.authorYEŞİL, GÖZDE
dc.contributor.authorGECKINLI, B. B.
dc.date.accessioned2021-03-03T12:47:17Z
dc.date.available2021-03-03T12:47:17Z
dc.identifier.citationGECKINLI B. B. , Toksoy G., SAYAR C., SÖYLEMEZ M. A. , YEŞİL G., AYDIN H., KARAMAN A., DEVRANOGLU B., "Prevalence of X-aneuploidies, X-structural abnormalities and 46, XY sex reversal in Turkish women with primary amenorrhea or premature ovarian insufficiency", EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY, cilt.182, ss.211-215, 2014
dc.identifier.issn0301-2115
dc.identifier.otherav_302491dc-9a05-46de-a280-4a24da1727dc
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/36850
dc.identifier.urihttps://doi.org/10.1016/j.ejogrb.2014.09.033
dc.description.abstractOur objective was to identify the distribution of cytogenetic abnormalities of 175 Turkish women with primary amenorrhea (PA) or premature ovarian insufficiency (POI). A retrospective study was performed using medical records of 94 patients with PA and 81 patients with POI at the Genetics Department, Zeynep Kamil Women's and Children's Research and Training Hospital, Istanbul, Turkey. G-banded metaphase kaiyotype analysis were prepared and analyzed. Chromosomal abnormalities were present in 44 of 175 cases (25%). 15 were full blown or mosaic numerical X chromosome abnormalities (8.5%), 10 were full blown or mosaic X-chromosome structural anomalies (5.7%), one was X-autosome translocation (0.5%), 3 were autosomal anomalies (1.7%), 12 were XY kaiyotype (6.8%), one was 45,X/46,XY mosaic and 2 were full blown or mosaic structural anomalies of Y chromosome (1.7%). The prevalence of chromosomal abnormalities was 25% in this large series of Turkish women with primary amenorrhea or premature ovarian insufficiency, most cases involving X-aneuploidy or X-structural abnormalities or 46,XY karyotype. High prevalence of chromosomal abnormalities is associated with POI starting at an early age (average age: 26 years). (C) 2014 Elsevier Ireland Ltd. All rights reserved.
dc.language.isoeng
dc.subjectTemel Bilimler
dc.subjectKADIN HASTALIKLARI & DOĞUM
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectÜREME BİYOLOJİSİ
dc.subjectBiyoloji ve Biyokimya
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.subjectBiyokimya
dc.subjectCerrahi Tıp Bilimleri
dc.subjectKadın Hastalıkları ve Doğum
dc.subjectYaşam Bilimleri
dc.titlePrevalence of X-aneuploidies, X-structural abnormalities and 46, XY sex reversal in Turkish women with primary amenorrhea or premature ovarian insufficiency
dc.typeMakale
dc.relation.journalEUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY
dc.contributor.departmentBezmiâlem Vakıf Üniversitesi , Tıp Fakültesi , Dahili Tıp Bilimleri Bölümü
dc.identifier.volume182
dc.identifier.startpage211
dc.identifier.endpage215
dc.contributor.firstauthorID99384


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