POLYPLOIDY PHENOMENON AS A CAUSE OF EARLY MISCARRIAGES IN ABORTION MATERIALS
Yildirim ME, Karakus S, Kurtulgan HK, Ozer L, Celik SB
*Corresponding Author: Malik Ejder Yildirim, Associate Professor. Department of Medical Genetics, Faculty of Medicine, Sivas Cumhuriyet University, 58104 Sivas, Turkey. Phone: 03462581085, Email: nemalik2002@gmail.com
page: 5

REFERENCES

1. Wesselink AK, Wise LA, Hatch EE, Mikkelsen EM, Savitz DA, Kirwa K, et al. A Prospective Cohort Study of Seasonal Variation in Spontaneous Abortion. Epidemiology. 2022; 33(3): 441-448. 2. Schmidt-Hansen M, Cameron S, Lord J, Hasler E. Initiation of abortion before there is definitive ultrasound evidence of intrauterine pregnancy: A systematic review with meta-analyses. Acta Obstet Gynecol Scand. 2020; 99(4): 451-458. 3. Woolner AMF, Raja EA, Bhattacharya S, Danielian P, Bhattacharya S. Inherited susceptibility to miscarriage: a nested case-control study of 31,565 women from an intergenerational cohort. Am J Obstet Gynecol. 2020; 222: 168.e1-168.e8. 4. Rolnik DL, Carvalho MH, Catelani AL, Pinto AP, Lira JB, Kusagari NK, et al. [Cytogenetic analysis of miscarriage material from spontaneous abortion]. Rev Assoc Med Bras. 2010; 56(6): 681-683. 5. Kim JW, Lyu SW, Sung SR, Park JE, Cha DH, Yoon TK, et al. Molecular analysis of miscarriage products using multiplex ligation-dependent probe amplification (MLPA): alternative to conventional karyotype analysis. Arch Gynecol Obstet. 2015; 291(2): 347–354. 6. Carp H, Toder V, Aviram A, Daniely M, Mashiach S, Barkai G. Karyotype of the abortus in recurrent miscarriage. Fertil Steril. 2001; 75(4): 678-682. 7. Pinar MH, Gibbins K, He M, Kostadinov S, Silver R. Early Pregnancy Losses: Review of Nomenclature, Histopathology, and Possible Etiologies. Fetal Pediatr Pathol. 2018; 37(3): 191-209. 8. Colley E, Hamilton S, Smith P, Morgan NV, Coomarasamy A, Allen S. Potential genetic causes of miscarriage in euploid pregnancies: a systematic review. Hum Reprod Update. 2019; 25(4): 452-472. 9. Ljunger E, Cnattingius S, Lundin C, Annerén G. Chromosomal anomalies in first-trimester miscarriages. Acta Obstet Gynecol Scand. 2005; 84(11): 1103-1107. 10. Du Y, Chen L, Lin J, Zhu J, Zhang N, Qiu X, et al. Chromosomal karyotype in chorionic villi of recurrent spontaneous abortion patients. Biosci Trends. 2018; 12(1): 32-39. 11. Robinson WP, McFadden DE, Stephenson MD. The origin of abnormalities in recurrent aneuploidy/polyploidy. Am J Hum Genet. 2001; 69(6): 1245-1254. 12. Nguyen BT, Chang EJ, Bendikson KA. Advanced paternal age and the risk of spontaneous abortion: an analysis of the combined 2011-2013 and 2013- 2015 National Survey of Family Growth. Am J Obstet Gynecol. 2019; 221(5): 476.e1-476.e7. 13. Jia CW, Wang L, Lan YL, Song R, Zhou LY, Yu L, et al. Aneuploidy in Early Miscarriage and its Related Factors. Chin Med J (Engl). 2015; 128(20): 2772-2776. 14. Toufaily MH, Roberts DJ, Westgate MN, Holmes LB. Triploidy: Variation of Phenotype. Am J Clin Pathol. 2016; 145(1): 86-95. 15. Wada Y, Kakiuchi S, Mizuguchi K, Nakamura T, Ito Y, Sago H, et al. A female newborn having mosaicism with near-tetraploidy and trisomy 18. Am J Med Genet A. 2016; 170A(5): 1262-1267. 16. Shah MS, Cinnioglu C, Maisenbacher M, Comstock I, Kort J, Lathi RB. Comparison of cytogenetics and molecular karyotyping for chromosome testing of miscarriage specimens. Fertil Steril. 2017; 107(4): 1028-1033. 17. Magnus MC, Hockey RL, Håberg SE, Mishra GD. Prepregnancy lifestyle characteristics and risk of miscarriage: the Australian Longitudinal Study on Women’s Health. BMC Pregnancy Childbirth. 2022; 22(1): 169. 18. Bastos R, Ramalho C, Dória S. [Prevalence of chromosomal abnormalities in spontaneous abortions or fetal deaths]. Acta Med Port. 2014; 27(1) :42-48. 19. Babu R, Van Dyke DL, Bhattacharya S, Dev VG, Liu M, Kwon M, et al. A rapid and reliable chromosome analysis method for products of conception using interphase nuclei. Mol Genet Genomic Med. 2018; 6(3): 370-381. 20. Pylyp LY, Spynenko LO, Verhoglyad NV, Mishenko AO, Mykytenko DO, Zukin VD. Chromosomal abnormalities in products of conception of first-trimester miscarriages detected by conventional cytogenetic analysis: a review of 1000 cases. J Assist Reprod Genet. 2018; 35(2): 265–271. 21. Turki RF, Assidi M, Banni HA, Zahed HA, Karim S, Schulten H, et al. Associations of recurrent miscarriages with chromosomal abnormalities, thrombophilia allelic polymorphisms and/or consanguinity in Saudi Arabia. BMC Med Genet. 2016; 17(Suppl 1): 69. 22. Shen J, Wu W, Gao C, Ochin H, Qu D, Xie J, et al. Chromosomal copy number analysis on chorionic villus samples from early spontaneous miscarriages by high throughput genetic technology. Mol Cytogenet. 2016; 9: 7. 23. Gug C, Burada F, Ioana M, Riza AL, Moldovan M, Mozos I, et al. Polyploidy in First and Second Trimester Pregnancies in Romania - a Retrospective Study. Clin Lab. 2020; 66(4). doi: 10.7754/Clin. Lab.2019.190649 24. Russo R, Sessa AM, Fumo R, Gaeta S. Chromosomal anomalies in early spontaneous abortions: interphase FISH analysis on 855 FFPE first trimester abortions. Prenat Diagn. 2016; 36(2): 186-191. 25. Brancati F, Mingarelli R, Dallapiccola B. Recurrent triploidy of maternal origin. Eur J Hum Genet. 2003; 11(12): 972-974. 26. Carson JC, Hoffner L, Conlin L, Parks WT, Fisher RA, Spinner N, et al. Diploid/triploid mixoploidy: A consequence of asymmetric zygotic segregation of parental genomes. Am J Med Genet A. 2018; 176(12): 2720-2732. 27. Kolarski M, Ahmetovic B, Beres M, Topic R, Nikic V, Kavecan I, et al. Genetic Counseling and Prenatal Diagnosis of Triploidy During the Second Trimester of Pregnancy. Med Arch. 2017; 71(2): 144-147. 28. Dória S, Lima V, Carvalho B, Moreira ML, Sousa M, Barros A, et al. Application of touch FISH in the study of mosaic tetraploidy and maternal cell contamination in pregnancy losses. J Assist Reprod Genet. 2010; 27(11): 657-662. 29. Soler A, Badenas C, Margarit E, Madrigal I, Muñoz M, Borobio V, et al. A 92, XXXY Miscarriage Consecutive to a Digynic Triploid Pregnancy. Cytogenet Genome Res. 2016; 149(4): 258-261. 30. Stefanova I, Jenderny J, Kaminsky E, Mannhardt A, Meinecke P, Grozdanova L, et al. Mosaic and complete tetraploidy in live-born infants: two new patients and review of the literature. Clin Dysmorphol. 2010; 19(3): 123-127. 31. Lee JM, Shin SY, Kim GW, Kim WJ, Wie JH, Hong S, et al. Optimizing the Diagnostic Strategy to Identify Genetic Abnormalities in Miscarriage. Mol Diagn Ther. 2021; 25(3): 351-359. 32. Gug C, Rațiu A, Navolan D, Drăgan I, Groza IM, Păpurică M, et al. Incidence and Spectrum of Chromosome Abnormalities in Miscarriage Samples: A Retrospective Study of 330 Cases. Cytogenet Genome Res. 2019; 158(4): 171-183. 33. Lathi RB, Gray Hazard FK, Heerema-McKenney A, Taylor J, Chueh JT. First trimester miscarriage evaluation. Semin Reprod Med. 2011; 29(6): 463-9. 34. Oliveira AF, Torrão MM, Nogueira R, Ferreira M. Recurrent fetal triploidy: is there a genetic cause? BMJ Case Rep. 2021; 14(3): e239843. 35. Xu Q, Chan Y, Feng Y, Zhu B, Yang B, Zhu S, et al. Factors associated with fetal karyotype in spontaneous abortion: a case-case study. BMC Pregnancy Childbirth. 2022; 22(1): 320. doi: 10.1186/s12884- 022-04491-8. 36. Massalska D, Ozdarska K, Roszkowski T, Bijok J, Kucińska-Chahwan A, Panek GM, et al. Distribution of diandric and digynic triploidy depending on gestational age. J Assist Reprod Genet. 2021; 38(9): 2391-2395. 37. Zaragoza MV, Surti U, Redline RW, Millie E, Chakravarti A, Hassold TJ. Parental origin and phenotype of triploidy in spontaneous abortions: predominance of diandry and association with the partial hydatidiform mole. Am J Hum Genet. 2000; 66(6): 1807-20. 38. Wiener-Megnazi Z, Auslender R, Dirnfeld M. Advanced paternal age and reproductive outcome. Asian J Androl. 2012; 14(1): 69-76.



Number 27
VOL. 27 (2), 2024
Number 27
VOL. 27 (1), 2024
Number 26
Number 26 VOL. 26(2), 2023 All in one
Number 26
VOL. 26(2), 2023
Number 26
VOL. 26, 2023 Supplement
Number 26
VOL. 26(1), 2023
Number 25
VOL. 25(2), 2022
Number 25
VOL. 25 (1), 2022
Number 24
VOL. 24(2), 2021
Number 24
VOL. 24(1), 2021
Number 23
VOL. 23(2), 2020
Number 22
VOL. 22(2), 2019
Number 22
VOL. 22(1), 2019
Number 22
VOL. 22, 2019 Supplement
Number 21
VOL. 21(2), 2018
Number 21
VOL. 21 (1), 2018
Number 21
VOL. 21, 2018 Supplement
Number 20
VOL. 20 (2), 2017
Number 20
VOL. 20 (1), 2017
Number 19
VOL. 19 (2), 2016
Number 19
VOL. 19 (1), 2016
Number 18
VOL. 18 (2), 2015
Number 18
VOL. 18 (1), 2015
Number 17
VOL. 17 (2), 2014
Number 17
VOL. 17 (1), 2014
Number 16
VOL. 16 (2), 2013
Number 16
VOL. 16 (1), 2013
Number 15
VOL. 15 (2), 2012
Number 15
VOL. 15, 2012 Supplement
Number 15
Vol. 15 (1), 2012
Number 14
14 - Vol. 14 (2), 2011
Number 14
The 9th Balkan Congress of Medical Genetics
Number 14
14 - Vol. 14 (1), 2011
Number 13
Vol. 13 (2), 2010
Number 13
Vol.13 (1), 2010
Number 12
Vol.12 (2), 2009
Number 12
Vol.12 (1), 2009
Number 11
Vol.11 (2),2008
Number 11
Vol.11 (1),2008
Number 10
Vol.10 (2), 2007
Number 10
10 (1),2007
Number 9
1&2, 2006
Number 9
3&4, 2006
Number 8
1&2, 2005
Number 8
3&4, 2004
Number 7
1&2, 2004
Number 6
3&4, 2003
Number 6
1&2, 2003
Number 5
3&4, 2002
Number 5
1&2, 2002
Number 4
Vol.3 (4), 2000
Number 4
Vol.2 (4), 1999
Number 4
Vol.1 (4), 1998
Number 4
3&4, 2001
Number 4
1&2, 2001
Number 3
Vol.3 (3), 2000
Number 3
Vol.2 (3), 1999
Number 3
Vol.1 (3), 1998
Number 2
Vol.3(2), 2000
Number 2
Vol.1 (2), 1998
Number 2
Vol.2 (2), 1999
Number 1
Vol.3 (1), 2000
Number 1
Vol.2 (1), 1999
Number 1
Vol.1 (1), 1998

 

 


 About the journal ::: Editorial ::: Subscription ::: Information for authors ::: Contact
 Copyright © Balkan Journal of Medical Genetics 2006