Cytogenetic Findings of Patients with Amenorrhea in Turkish Population: A Retrospective Study
Yazarlar (6)
Nurten Kara
Ondokuz Mayis Üniversitesi, Türkiye
Ondokuz Mayis Üniversitesi, Türkiye
Prof. Dr. Sengul Tural Ondokuz Mayis Üniversitesi, Türkiye
Mehmet Elbistan
Ondokuz Mayis Üniversitesi, Türkiye
Ondokuz Mayis Üniversitesi, Türkiye
Doç. Dr. Nevin KARAKUŞ Ondokuz Mayis Üniversitesi, Türkiye
Prof. Dr. Davut Guven Ondokuz Mayis Üniversitesi, Türkiye
Prof. Dr. Idris Kocak Ondokuz Mayis Üniversitesi, Türkiye
| Makale Türü | Özgün Makale (ESCI dergilerinde yayınlanan tam makale) | ||
| Dergi Adı | International Journal of Human Genetics | ||
| Dergi ISSN | 0972-3757 Wos Dergi Scopus Dergi | ||
| Makale Dili | İngilizce | Basım Tarihi | 06-2012 |
| Cilt / Sayı / Sayfa | 12 / 2 / 87–92 | DOI | 10.1080/09723757.2012.11886167 |
| Makale Linki | https://www.researchgate.net/profile/Sengul-Tural/publication/233790899_Cytogenetic_Findings_of_Patients_with_Amenorrhea_in_Turkish_Population_A_Retrospective_Study/links/0912f50b87b058b238000000/Cytogenetic-Findings-of-Patients-with-Amenorrhea-in-Tu | ||
| UAK Araştırma Alanları |
Tıbbi Biyoloji
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| Özet |
| We performed a retrospective study, with the purpose of establishing the frequency of chromosomal anomalies in amenorrhea cases referred to our genetic laboratory from hospitals in the Middle Black Sea of Turkey. In this study, 105 cases with amenorrhea were analysed and evaluated by Department of Medical Biology and Medical Genetics. Karyotype analyses of cases were made from their peripheral blood lymphocytes by standard method. Twenty metaphases had been prepared with GTG banding method for each patient was analyzed. When a mosaic karyotype was found in any case approximately 100 cells were examined. Chromosomal anomaly was found in 15 (14.3%) patients. Chromosome anomalies in 15 cases were as follows; 34% 45, X, 13.2% 46, XY (testicular feminization), 6.6% mosaic 45, X/46, XX, 6.6% 45, X, del (Xq21), 6.6% 45, X, del (Xp)(p11. 21)/45, X, 6.6% 45, X/46, X, der (X), 6.6% t (X; 6), 6.6% t (X; 14), 11.76% 46, X, iX (q)(10)/45, X. The most common chromosomal abnormalities in cases with amenorrhea were monosomy X and different structural abnormalities of X chromosome respectively. |
| Anahtar Kelimeler |
| Amenorrhea | Chromosomal abnormalities | Cytogenetics | Menstruation | Secondary sexual characteristics |
BM Sürdürülebilir Kalkınma Amaçları
| Atıf Sayıları | |
| Web of Science | 7 |
| Scopus | 9 |
| Google Scholar | 12 |