Gamete donor karyotyping: Between real usefulness and safety rules;Le caryotype systématique chez les donneurs et donneuses de gamètes: Utilité réelle ou simple sécurité?

Gynecologie Obstetrique et Fertilite

Volumn 32, Issue 9, 2004, Pages 803-812

  Siffroi, J P ^a  

^a HÔPITAL TENON   (France)

Author keywords

Caryotype; CECOS; Don de sperme; Don dovocytes; Egg donation; Karyotype; Sperm donation

Indexed keywords

ARTICLE; CHROMOSOME 9; CHROMOSOME ABERRATION; CHROMOSOME TRANSLOCATION; GAMETE; HUMAN; KARYOTYPE 46,XX; KARYOTYPE 47,XXX; KARYOTYPE 47,XYY; KARYOTYPING; QUESTIONNAIRE; SPERM; Y CHROMOSOME;

EID: 4544271419     PISSN: 12979589     EISSN: 17696682     Source Type: Journal    
DOI: 10.1016/j.gyobfe.2004.08.008     Document Type: Article

References (28)

1. P. Albert, C. Leonard, J. Selva, and G. David Genetic aspects of artificial insemination with donor semen: the French CECOS Federation guidelines Am. J. Med. Genet. 33 1989 269 275
2. American Society for Reproductive Medicine 2002 guidelines for gamete and embryo donation Fertil. Steril. 77 suppl. 5 2002 S2 S5 S6S8
3. American Society for Reproductive Medicine Minimal genetic screening for gamete donors Fertil. Steril. 77 suppl. 5 2002 S15 S16
4. J. Nielsen, and M. Wohlert Chromosome abnormalities found among 34910 newborn children: results from a 13-year incidence study in Arhus, Denmark Hum. Genet. 87 1991 81 83
5. M.R. Guichaoua, D. Delafontaine, B. Nol, and J.M. Luciani Linfertilit masculine dorigine chromosomique Contracept. Fertil. Sex. 21 1993 113 121
6. N. Pandiyan, and A.M. Jequier Mitotic chromosomal anomalies among 1210 infertile men Hum. Reprod. 11 1996 2604 2608
7. A. Yoshida, K. Ueda, K. Nagao, H. Hara, N. Ishii, and K. Miura Cytogenetic survey of 1,007 infertile males Urol. Int. 58 1997 166 176
8. D. Meschede, B. Lemcke, J.R. Exeler, C.H. De Geyter, H.M. Behre, and E. Nieschlag Chromosome abnormalities in 447 couples undergoing intracytoplasmic sperm injection prevalence, types, sex distribution and reproductive relevance Hum. Reprod. 13 1998 576 582
9. B. Peschka, J.L. Leygraaf, K. Van der Ven, M. Montag, B. Schartmann, and R. Schubert Type and frequency of chromosome aberrations in 781 couples undergoing intracytoplasmic sperm injection Hum. Reprod. 14 1999 2257 2263
10. J. Gekas, F. Thpot, C. Turleau, J.P. Siffroi, J.P. Dadoune, and R. Wasels Chromosomal factors of infertility in candidate couples for ICSI: an equal risk of constitutional aberrations in women and men Hum. Reprod. 16 2001 82 90
11. S. Ogawa, S. Araki, Y. Araki, M. Ohno, and I. Sato Chromosome analysis of human spermatozoa from an oligoasthenozoospermic carrier for a 13;14 Robertsonian translocation by their injection into mouse oocytes Hum. Reprod. 15 2000 1136 1139
12. N. Frydman, S. Romana, M. Le Lorch, M. Vekemans, R. Frydman, and G. Tachdjian Assisting reproduction of infertile men carrying a Robertsonian translocation Hum. Reprod. 16 2001 2274 2277
13. T. Escudero, M. Lee, D. Carrel, J. Blanco, and S. Munn Analysis of chromosome abnormalities in sperm and embryos from two 45,XY,t(13;14) (q10;q10) carriers Prenat. Diagn. 20 2000 599 602
14. P.N. Scriven, F.A. Flinter, P.R. Braude, and C. Mackie Ogilvie Robertsonian translocations reproductive risks and indications for preimplantation genetic diagnosis Hum. Reprod. 16 2001 2267 2273
15. L. Gianaroli, M.C. Magli, A.P. Ferraretti, S. Munn, B. Balicchia, and T. Escudero Possible interchromosomal effect in embryos generated by gametes from translocation carriers Hum. Reprod. 17 2002 3201 3207
16. T. Eggermann, and K. Zerres Uniparental disomy and Robertsonian translocations: risk estimation and prenatal testing Mol. Diagn. 7 2003 113 117
17. C. Chu, S. Schwartz, and E. Mc Pherson Paternal uniparental isodisomy for chromosome 14 in a patient with a normal 46,XY karyotype Am. J. Med. Genet. 127A 2004 167 171
18. F. Pellestor, I. Imbert, B. Andreo, and G. Lefort Study of the occurrence of interchromosomal effect in spermatozoa chromosomal rearrangement carriers by fluorescence in-situ hybridization and primed in-situ labelling techniques Hum. Reprod. 16 2001 1155 1164
19. C. Cans, O. Cohen, M.A. Mermet, J. Demongeot, and P. Jalbert Human reciprocal translocations: is the unbalanced mode at birth predictable? Hum. Genet. 91 1993 228 232
20. C. Cans, O. Cohen, C. Lavergne, M.A. Mermet, J. Demongeot, and P. Jalbert Logistic regression model to estimate the risk of unbalanced offspring in reciprocal translocations Hum. Genet. 92 1993 598 604
21. O. Cohen, C. Cans, M.A. Mermet, J. Demongeot, and P. Jalbert Viability thresholds for partial trisomies and monosomies. A study of 1,159 viable unbalanced reciprocal translocations Hum. Genet. 93 1994 188 194
22. N. Rives, G. Joly, A. Machy, N. Simon, P. Leclerc, and B. Mac Assessment of sex chromosome aneuploidy in sperm nuclei from 47,XXY and 46,XY/47,XXY males: comparison with fertile and infertile males with normal karyotypes Mol. Hum. Reprod. 6 2000 107 112
23. E. Chevret, S. Rousseaux, M. Monteil, Y. Usson, J. Cozzi, and R. Pelletier Meiotic behaviour of sex chromosomes investigated by three-colour FISH on 35 142 sperm nuclei from two 47,XYY males Hum. Genet. 99 1997 407 412
24. Q. Shi, and R. Martin Multicolor fluorescence in situ hybridization analysis of meiotic chromosome segregation in a 47,XYY male and review of the literature Am. J. Med. Genet. 93 2000 40 46
25. J.Y. Wang, O. Samura, D.K. Zhen, J.M. Cowan, V. Cardone, and M. Summers Fluorescence in situ hybridization analysis of chromosomal constitution in spermatozoa from a mosaic 47,XYY/46,XY male Mol. Hum. Reprod. 6 2000 665 668
26. N. Rives, N. Simon, J.P. Milazzo, C. Barthlmy, and B. Mac Meiotic segregation of sex chromosomes in mosaic and non-mosaic XYY males: case reports and review of the literature Int. J. Androl. 26 2003 242 249
27. J.H. Tuerlings, H.F. De France, A. Hamers, R. Hordijk, J.O. Van Hemel, and K. Hansson Chromosome studies in 1792 males prior to intracytoplasmic sperm injection: the Dutch experience Eur. J. Hum. Genet. 6 1998 194 200
28. K. Eggermann, U.A. Mau, G. Bujdoso, E. Koltai, H. Engels, and R. Schubert Supernumerary marker chromosomes derived from chromosome 15: analysis of 32 new cases Clin. Genet. 62 2002 89 93