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Prenatal diagnosis of triploidy in second trimester of pregnancy: a series of 4 cases over an eleven-year period / Diagnosticul prenatal al triploidiei în trimestrul al II-lea de sarcină: o serie de patru cazuri depistate în unsprezece ani Cover

Prenatal diagnosis of triploidy in second trimester of pregnancy: a series of 4 cases over an eleven-year period / Diagnosticul prenatal al triploidiei în trimestrul al II-lea de sarcină: o serie de patru cazuri depistate în unsprezece ani

Open Access
|Jun 2015

References

  1. 1. Snijders RJM, Sebire NJ, Nicolaides KH. Maternal age and gestational age-specific risk for chromosomal defects. Fetal Diagn Ther. 1995;10(6):356-67. DOI: 10.1159/000264259 DOI: 10.1159/00026425810.1159/0002642598579773
  2. 2. McKinlay Gardner RJ, Sutherland GR. Chromosome abnormalities detected at prenatal diagnosis, McKinlay Gardner RJ, Sutherland GR (eds). in Chromosome abnormalities and genetic counselling, 3th ed. Oxford University Press Inc. New York 2004;392-434.
  3. 3. Wick JB, Johnson KJ, O`Brian J, Wick MJ. Second trimester diagnosis of triploidy: a series of four cases. Am J Perinatol Rep. 2013;3(1):37-40.
  4. 4. McFadden DE, Robinson WP. Phenotype of triploid embryos. J Med Genet. 2006;43(7):609-12. DOI: 10.1136/jmg.2005.03774710.1136/jmg.2005.037747256455616236813
  5. 5. Egozcue S, Blanco J, Vidal F, Egozcue J. Diploid sperm and the origin of triploidy. Hum Reprod. 2002;17(1):5-7. DOI: 10.1093/humrep/17.1.510.1093/humrep/17.1.511756352
  6. 6. Wang BT, Chong TP, Boyar FZ, Kopita KA, Ross LP, El-Naggar MM. et al. Abnormalities in spontaneous abortions detected by G-banding and chromosomal microarray analysis (CMA) at a national reference laboratory. Mol Cytogenet. 2014;7:33. DOI: 10.1186/1755-8166-7-3310.1186/1755-8166-7-33404949524914406
  7. 7. Wellesley D, Dolk H, Boyd PA, Greenlees R, Haeusler M, Nelen V, et al. Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population- based congenital anomaly registers in Europe. Eur J Hum Genet. 2012;20(5):521-6. DOI: 10.1038/ ejhg.2011.24610.1038/ejhg.2011.246333022422234154
  8. 8. Iliopoulos D, Vassiliou G, Sekerli E, Sidiropoulou V, Tsiga A, Dimopoulou A, et al. Long survival in a 69,XXX triploid infant in Greece. Genet Mol Res. 2005;4(4):755-9.
  9. 9. Guanciali-Franchi P, Iezzi I, Matarrelli B, Morizio E, Calabrese G, Palka G. A case of triploidy detected by crosstrimester test. J Prenat Med. 2012;6(3):55-6.
  10. 10. Bagherizadeh E, Oveisi M, Hadipour Z, Saremi A, Shafaghati Y, Behjati F. Triploidy in a fetus following amniocentesis referred for maternal serum screening test at second trimester. Indian J Hum Genet. 2010;16(2):94-6. DOI: 10.4103/0971-6866.6937110.4103/0971-6866.69371295595821031058
  11. 11. Wapner RJ, Martin CL, Levy B, Ballif BC, Eng CM, Zachary JM, et al. Chromosomal microarray ver Med. 2012;367(23):2175-84. DOI: 10.1056/NEJMoa120338210.1056/NEJMoa1203382354941823215555
  12. 12. Dalmia R, Young P, Sunanda GV. A case of triploidy. Fertil Steril. 2005;83(2):462-3. DOI: 10.1016/j.fertnstert. 2004.07.968
  13. 13. Brancati F, Mingarelli R, Dallapiccola B. Reccurent triploidy of maternal origin. Eur J Human Genet. 2003;11(12):972-4. DOI: 10.1038/sj.ejhg.520107610.1038/sj.ejhg.520107614508508
  14. 14. Daniel A, Wu Z, Benetts B, Slater H, Osborn R, Jackson J. Karyotype, phenotype and parental origin in 19 cases of triploidy. Prenat Diagn. 2001;21(12):1034-48. DOI: 10.1002/pd.16410.1002/pd.16411746161
  15. 15. Falcon O, Peralta CFA, Cavoretto P, Auer M, Nicolaides KH. Fetal trunk and head volume in chromosomally abnormal fetuses at 11 + 0 to 13 + 6 weeks of gestation. Ultrasound Obstet Gynecol. 2005;26(5):517-20. DOI: 10.1002/uog.199010.1002/uog.199016142826
  16. 16. Baumer A, Balmer D, Binkert F, Schinzel A. Parental origin and mechanisms of formation of triploidy: a study of 25 cases. Eur J Hum Genet. 2000;8(12):911-7. DOI: 10.1038/sj.ejhg.520057210.1038/sj.ejhg.520057211175278
  17. 17. Witters I, Van Robays J, Willekes C, Coumans A, Peeters H, Gyselaers W, et al. Trisomy 13, 18, 21, triploidy and Turner syndrome: the 5T’s. Look at the hands. Facts Views Vis Obgyn. 2011;3(1):15-21.
  18. 18. Lapaire O, Lu XY, Johnson KL, Jarrah Z, Stroh H, Cowan JM. Array-CGH analysis of cell-free fetal DNA in 10 mL of amniotic fluid supernatant. Prenat Diagn. 2007;27(7):616-21. DOI: 10.1002/pd.175210.1002/pd.175217510923
  19. 19. Chiu RW, Lo YM. Noninvasive prenatal diagnosis empowered by high-throughput sequencing. Prenat Diagn. 2012;32(4):401-6. DOI: 10.1002/pd.3822 10.1002/pd.382222467171
DOI: https://doi.org/10.1515/rrlm-2015-0014 | Journal eISSN: 2284-5623 | Journal ISSN: 1841-6624
Language: English
Page range: 213 - 220
Submitted on: Nov 12, 2014
Accepted on: Apr 13, 2015
Published on: Jun 23, 2015
Published by: Romanian Association of Laboratory Medicine
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year

© 2015 Demetra Socolov, Elena Mihălceanu, Diana Popovici, Eusebiu Vlad Gorduza, Raluca Balan, Violeta Martiniuc, Răzvan Socolov, published by Romanian Association of Laboratory Medicine
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.