BibTex RIS Kaynak Göster

Recurrent spontaneous abortions in a family with balanced resiprocal translocation 46,XY,t(1;15) (p35: q11.1): Case report

Yıl 2009, Cilt: 40 Sayı: 2, 75 - 77, 01.03.2009

Öz

Balanced resiprocal translocations (RT) constitute the major group of chromosomal abnormalities responsible for recurrent spontaneous abortions (rsa). In this study, we aimed to emphasize the importance ofpreimplantation genetic diagnosis and assisted reproductive techniques to obtain healthy embryos in a couple with 5 abortions in their reproductive history.

Kaynakça

  • 1. Edmonds DK, Lindsay KS, Miller JF, et al. Early embryonic mortality inwomen. Fertil Steril 1982; 38:447-453
  • 2. Wilcox AJ, Weinberg CR, O 'Connor JF, et al
  • Incidence of early loss of pregnancy. N Engl J Med 1988; 319:189-194
  • 3. Jacobs PA, Hassold T. Chromosome abnormalities: origin and etiology in abortions and livebirths. In: Vogel F, Sperling K, eds. Human Genetics. Berlin: Springer-Verlag; 1987; 233-244
  • 4. Roman E. Fetal loss rates and theirrelation to pregnancy order. J Epidemiol Community Health 1984; 38: 29-35
  • 5. Hatasaka HH. Recurrent miscarriage: epidemiological factors, definitions, and incidence
  • Clin Obstet Gynecol 1994; 37; 625-634
  • 6. Dewalds GW and Michels WW. Recurrent miscarriages: cytogenetic causes and genetic counseling of affected families. Clin Obstet Gynecol 1986; 29: 865-885
  • 7. Byrne J.L.C. and Ward W. Genetic factors in recurrent abortion. Clin Obstet Gynecol 1994; 37: 693-704
  • 8. Sugiura-Ogasawara M, Ozaki Y, Sato T, et al
  • Poor prognosis of recurrent aborters with either maternal or paternal reciprocal translocations
  • Fertil Steril. 2004; 81: 367-373
  • 9. Goddijn M, Joosten JH, Knegt AC, et al. Clinical relevance of diagnosing structural: chromosome abnormalities in couples with repeated miscarriage
  • Hum Reprod. 2004; 19:1013-1017
  • 10. Stephenson MD, Sierra S. Reproductive outcomes in recurrent pregnancy loss associated with a parental carrier of a structural chromosome rearrangement. HumReprod. 2006; 21:1076-1082
  • 11. Stephenson M, and Kutteh W. Evaluation and Management of Recurrent Early Pregnancy Loss
  • Clinical Obstetrics and Gynecology 2007; 50(l):132-145
  • 12. Nussbaum, Mclnnes, Willard: Genetics in Medicine, 6th (eds). Saunders Press 2004; 148-149
  • 13. Balcı A, Yirmibeş M, Bal F ve ark. Ailesel resiprokal translokasyon ve tekrarlayan düşükler
  • Perinataloji Dergisi, 1996;4;218-219
  • 14. Haidl G., Peschka B., Schwanitz G., Montag M., van der Ven K., van der Ven H. Cytogenetic and andrological status and ICSIresults in couples with severe malefactor infertility. Asian JAndrol, 2000;2: 293-296
  • 15. Montag M, van der Ven K, Ved S, Schmutzler A, Prietl G, Krebs D, et al. Success of intracytoplasmic sperm injection in couples with male and/or female chromosome aberrations. Hum Reprod 1997; 12:2635-40
  • 16. Mayumi SO, Ozaki Y, Sato T, Suzimori N, Suzumori K, Yamada A, et al: Poor prognosis of recurrent aborters with either maternal or paternal reciprocal translocations. Fertility and Sterility 2004; 81:31-4
  • 17. Munne S, Sandalinas M, Escudero T, Fung J, Gianoroli L, Cohen J: Outcome ofpreimplantation genetic diagnosis of translocations. Fertil Steril 2000; 73:1209-18

Tekrarlayan düşük öykülü ailede dengeli resiprokal translokasyon olgusu: 46,XY,t(l;15)(p35: qll.l)

Yıl 2009, Cilt: 40 Sayı: 2, 75 - 77, 01.03.2009

Öz

Dengeli resiprokal translokasyonlar (RT), çiftlerde tekrarlayan düşüklerden sorumlu olan kromozomal düzensizliklerin en büyük grubunu oluşturur. Bu çalışmamızda merkezimize re/ere edilen; reprodüktif öyküsünde 5 düşük olan çiftte yardımcı üreme teknikleri (YÜT) ve preimplantasyon genetik tanı (PGT) ile sağlıklı embryonun seçilerek gebelik elde edilmesinin önemini vurgulamayı amaçladık.

Kaynakça

  • 1. Edmonds DK, Lindsay KS, Miller JF, et al. Early embryonic mortality inwomen. Fertil Steril 1982; 38:447-453
  • 2. Wilcox AJ, Weinberg CR, O 'Connor JF, et al
  • Incidence of early loss of pregnancy. N Engl J Med 1988; 319:189-194
  • 3. Jacobs PA, Hassold T. Chromosome abnormalities: origin and etiology in abortions and livebirths. In: Vogel F, Sperling K, eds. Human Genetics. Berlin: Springer-Verlag; 1987; 233-244
  • 4. Roman E. Fetal loss rates and theirrelation to pregnancy order. J Epidemiol Community Health 1984; 38: 29-35
  • 5. Hatasaka HH. Recurrent miscarriage: epidemiological factors, definitions, and incidence
  • Clin Obstet Gynecol 1994; 37; 625-634
  • 6. Dewalds GW and Michels WW. Recurrent miscarriages: cytogenetic causes and genetic counseling of affected families. Clin Obstet Gynecol 1986; 29: 865-885
  • 7. Byrne J.L.C. and Ward W. Genetic factors in recurrent abortion. Clin Obstet Gynecol 1994; 37: 693-704
  • 8. Sugiura-Ogasawara M, Ozaki Y, Sato T, et al
  • Poor prognosis of recurrent aborters with either maternal or paternal reciprocal translocations
  • Fertil Steril. 2004; 81: 367-373
  • 9. Goddijn M, Joosten JH, Knegt AC, et al. Clinical relevance of diagnosing structural: chromosome abnormalities in couples with repeated miscarriage
  • Hum Reprod. 2004; 19:1013-1017
  • 10. Stephenson MD, Sierra S. Reproductive outcomes in recurrent pregnancy loss associated with a parental carrier of a structural chromosome rearrangement. HumReprod. 2006; 21:1076-1082
  • 11. Stephenson M, and Kutteh W. Evaluation and Management of Recurrent Early Pregnancy Loss
  • Clinical Obstetrics and Gynecology 2007; 50(l):132-145
  • 12. Nussbaum, Mclnnes, Willard: Genetics in Medicine, 6th (eds). Saunders Press 2004; 148-149
  • 13. Balcı A, Yirmibeş M, Bal F ve ark. Ailesel resiprokal translokasyon ve tekrarlayan düşükler
  • Perinataloji Dergisi, 1996;4;218-219
  • 14. Haidl G., Peschka B., Schwanitz G., Montag M., van der Ven K., van der Ven H. Cytogenetic and andrological status and ICSIresults in couples with severe malefactor infertility. Asian JAndrol, 2000;2: 293-296
  • 15. Montag M, van der Ven K, Ved S, Schmutzler A, Prietl G, Krebs D, et al. Success of intracytoplasmic sperm injection in couples with male and/or female chromosome aberrations. Hum Reprod 1997; 12:2635-40
  • 16. Mayumi SO, Ozaki Y, Sato T, Suzimori N, Suzumori K, Yamada A, et al: Poor prognosis of recurrent aborters with either maternal or paternal reciprocal translocations. Fertility and Sterility 2004; 81:31-4
  • 17. Munne S, Sandalinas M, Escudero T, Fung J, Gianoroli L, Cohen J: Outcome ofpreimplantation genetic diagnosis of translocations. Fertil Steril 2000; 73:1209-18
Toplam 24 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Bölüm Makaleler
Yazarlar

Nur Dokuzeylül Bu kişi benim

Semra Kahraman Bu kişi benim

Yayımlanma Tarihi 1 Mart 2009
Yayımlandığı Sayı Yıl 2009 Cilt: 40 Sayı: 2

Kaynak Göster

APA Dokuzeylül, N., & Kahraman, S. (2009). Tekrarlayan düşük öykülü ailede dengeli resiprokal translokasyon olgusu: 46,XY,t(l;15)(p35: qll.l). Zeynep Kamil Tıp Bülteni, 40(2), 75-77. https://doi.org/10.16948/zktb.31508
AMA Dokuzeylül N, Kahraman S. Tekrarlayan düşük öykülü ailede dengeli resiprokal translokasyon olgusu: 46,XY,t(l;15)(p35: qll.l). Zeynep Kamil Tıp Bülteni. Mart 2009;40(2):75-77. doi:10.16948/zktb.31508
Chicago Dokuzeylül, Nur, ve Semra Kahraman. “Tekrarlayan düşük öykülü Ailede Dengeli Resiprokal Translokasyon Olgusu: 46,XY,t(l;15)(p35: qll.L)”. Zeynep Kamil Tıp Bülteni 40, sy. 2 (Mart 2009): 75-77. https://doi.org/10.16948/zktb.31508.
EndNote Dokuzeylül N, Kahraman S (01 Mart 2009) Tekrarlayan düşük öykülü ailede dengeli resiprokal translokasyon olgusu: 46,XY,t(l;15)(p35: qll.l). Zeynep Kamil Tıp Bülteni 40 2 75–77.
IEEE N. Dokuzeylül ve S. Kahraman, “Tekrarlayan düşük öykülü ailede dengeli resiprokal translokasyon olgusu: 46,XY,t(l;15)(p35: qll.l)”, Zeynep Kamil Tıp Bülteni, c. 40, sy. 2, ss. 75–77, 2009, doi: 10.16948/zktb.31508.
ISNAD Dokuzeylül, Nur - Kahraman, Semra. “Tekrarlayan düşük öykülü Ailede Dengeli Resiprokal Translokasyon Olgusu: 46,XY,t(l;15)(p35: qll.L)”. Zeynep Kamil Tıp Bülteni 40/2 (Mart 2009), 75-77. https://doi.org/10.16948/zktb.31508.
JAMA Dokuzeylül N, Kahraman S. Tekrarlayan düşük öykülü ailede dengeli resiprokal translokasyon olgusu: 46,XY,t(l;15)(p35: qll.l). Zeynep Kamil Tıp Bülteni. 2009;40:75–77.
MLA Dokuzeylül, Nur ve Semra Kahraman. “Tekrarlayan düşük öykülü Ailede Dengeli Resiprokal Translokasyon Olgusu: 46,XY,t(l;15)(p35: qll.L)”. Zeynep Kamil Tıp Bülteni, c. 40, sy. 2, 2009, ss. 75-77, doi:10.16948/zktb.31508.
Vancouver Dokuzeylül N, Kahraman S. Tekrarlayan düşük öykülü ailede dengeli resiprokal translokasyon olgusu: 46,XY,t(l;15)(p35: qll.l). Zeynep Kamil Tıp Bülteni. 2009;40(2):75-7.