Preimplantation genetic diagnosis in female and male carriers of reciprocal translocations: Clinical outcome until delivery of 312 cycles

European Journal of Human Genetics

Volumn 20, Issue 4, 2012, Pages 376-380

  Keymolen, Kathelijn ^a   Staessen, Catherine ^a   Verpoest, Willem ^b   Liebaers, Inge ^a   Bonduelle, Maryse ^a  

^a UNIVERSITY HOSPITAL BRUSSELS   (Belgium)

^b CENTRE FOR REPRODUCTIVE MEDICINE   (Belgium)

Author keywords

PGD; preimplantation genetic diagnosis; reciprocal translocations; reproductive counseling

Indexed keywords

ADULT; ARTICLE; CLINICAL ASSESSMENT; DELIVERY; EMBRYO TRANSFER; FEMALE; FEMALE INFERTILITY; HETEROZYGOTE; HUMAN; LIVE BIRTH; MAJOR CLINICAL STUDY; MALE; MALE INFERTILITY; OUTCOME ASSESSMENT; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RECIPROCAL CHROMOSOME TRANSLOCATION; REPRODUCTIVE HISTORY; RETROSPECTIVE STUDY; SPONTANEOUS ABORTION; TWIN PREGNANCY;

ADULT; EMBRYO TRANSFER; FEMALE; GENETIC COUNSELING; HETEROZYGOTE; HUMANS; LIVE BIRTH; MALE; PREGNANCY; PREGNANCY COMPLICATIONS; PREIMPLANTATION DIAGNOSIS; RETROSPECTIVE STUDIES; TRANSLOCATION, GENETIC;

EID: 84858334604     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2011.208     Document Type: Article

References (28)

1. Iselius L, Lindsten J, Aurias A et al: The 11q;22q translocation: A collaborative study of 20 new cases and analysis of 110 families. Hum Genet 1983; 64: 343-355.
2. Kurahashi H, Inagaki H, Ohye T, Kogo H, Kato T, Emanuel BS: Chromosomal translocations mediated by palindromic DNA. Cell Cycle 2006; 5: 1297-1303.
3. Hamerton JL, Canning N, Ray M, Smith S: A cytogenetic survey of 14,069 newborn infants. Incidence of chromosome abnormalities. Clin Genet 1975; 8: 223-243.
4. Van Dyke DL, Weiss L, Robertson JR, Babu VR: The frequency and mutation rate of balanced autosomal rearrangements in man estimated from prenatal genetic studies for advanced maternal age. Am J Hum Genet 1983; 35: 301-308.
5. Fryns JP, Van Buggenhout G: Structural chromosome rearrangements in couples with recurrent fetal wastage. Eur J Obstet Gynecol 1998; 81: 171-176.
6. Meza-Espinoza JP, Anguiano LO, Rivera H: Chromosomal abnormalities in couples with reproductive disorders. Gynecol Obstet Invest. 2008; 66: 237-240.
7. Nussbaum RR, McInnes RR, Willard HF: Principles of clinical cytogenetics; in Thompson & Thompson Genetics in Medicine. Philadelphia: Saunders, 2007, 7th edn, pp 74-75.
8. Ogilvie CM, Braude P, Scriven PN: Successful pregnancy outcomes after preimplantation genetic diagnosis (PGD) for carriers of chromosome translocations. Hum Fertil (Camb.) 2001; 4: 168-171.
9. Harton GL, Harper JC, Coonen E, Pehlivan T, Vesela K, Wilton L: European Society for Human Reproduction and Embryology (ESHRE) PGD Consortium. ESHRE PGD consortium best practice guidelines for fluorescence in situ hybridization-based PGD. Hum Reprod 2011; 26: 25-32.
10. Vandervorst M, Liebaers I, Sermon K et al: Successful preimplantation genetic diagnosis is related to the number of available cumulus-oocyte complexes. Hum Reprod 1998; 13: 3169-3176.
11. Devroey P, Van Steirteghem A: A review of ten years experience of ICSI. Hum Reprod Update 2004; 10: 19-28.
12. Verpoest W, Haentjens P, De Rycke M et al: Cumulative reproductive outcome after preimplantation genetic diagnosis: A report on 1498 couples. Hum Reprod 2009; 24: 2951-2959.
13. De Vos A, Van Steirteghem A: Aspects of biopsy procedures prior to preimplantation genetic diagnosis. Prenat Diagn 2001; 21: 767-780.
14. Staessen C, Coonen E, Van Assche E et al: Preimplantation diagnosis for X and Y normality in embryos from three Klinefelter patients. Hum Reprod 1996; 11: 1650-1653.
15. Staessen C, Tournaye H, Van Assche E et al: PGD in 47,XXY Klinefelter's syndrome patients. Hum Reprod Update 2003; 9: 319-330.
16. Harper JC, Coonen E, De Rycke M et al: ESHRE PGD Consortium data collection X: Cycles from January to December 2007 with pregnancy follow-up to October 2008. Hum Reprod 2010; 25: 2685-2707.
17. Bonduelle M, Liebaers I, Deketelaere V et al: Neonatal data on a cohort of 2889 infants born after ICSI (1991-1999) and of 2995 infants born after IVF (1983-1999). Hum Reprod. 2002; 17: 671-694.
18. Keymolen K, Staessen C, Verpoest W et al: A proposal for reproductive counselling in carriers of Robertsonian translocations: 10 years of experience with preimplantation genetic diagnosis. Hum Reprod 2009; 24: 2365-2371.
19. De Rademaeker M, Verpoest W, De Rycke M et al: Preimplantation genetic diagnosis for myotonic dystrophy type 1: Upon request to child. Eur J Hum Genet 2009; 17: 1403-1410.
20. Buss L, Tolstrup J, Munk C et al: Spontaneous abortion: A prospective cohort study of younger women from the general population in Denmark. Validation, occurrence and risk determinants. Acta Obstet Gynecol Scand. 2006; 85: 467-475.
21. Ko DS, Cho JW, Park SY et al: Clinical outcomes of Preimplantation Genetic Diagnosis (PGD) and Analysis of Meiotic Segregation Modes in Reciprocal Translocation Carriers. Am J Med Genet Part A 2010; 152A: 1428-1433.
22. Fischer J, Colls P, Escudero T, Munné S: Preimplantation genetic diagnosis (PGD) improves pregnancy outcome for translocation carriers with a history of recurrent losses. Fertil Steril 2010; 94: 283-289.
23. Goossens V, Harton G, Mouton C, Traeger-Synodinos J, Van Rij M, Harper J: ESHRE PGD Consortium data collection IX: Cycles from January to December 2006 with pregnancy follow-up to October 2007. Hum Reprod 2009; 24: 1786-1810.
24. Bonduelle M, Wennerholm UB, Loft A et al: A multi-centre cohort study of the physical health of 5-year-old children conceived after intracytoplasmic sperm injection, in vitro fertilization and natural conception. Hum Reprod 2005; 20: 413-419.
25. Desmyttere S, Verpoest W, De Rycke M et al: Neonatal outcome of 995 children conceived after embryo biopsy compared to children born after intracytoplasmic sperm injection. Hum Reprod 2010; 25(Suppl 1): 2945-2950.
26. Dolk H, Loane M, Garne E: The prevalence of congenital anomalies in Europe. Adv Exp Med Biol 2010; 686: 349-364.
27. Sugiura-Ogasawara M, Aoki K, Fujii T et al: Subsequent pregnancy outcomes in recurrent miscarriage patients with a paternal or maternal carrier of a structural chromosome rearrangement. J Hum Genet 2008; 53: 622-628.
28. Gianaroli L, Magli MC, Ferraretti AP et al: Possible interchromosomal effect in embryos generated by gametes from translocation carriers. Hum Reprod 2002; 17: 3201-3207.