Predictive value of sperm fluorescence in situ hybridization analysis on the outcome of preimplantation genetic diagnosis for translocations

Fertility and Sterility

Volumn 79, Issue SUPPL. 3, 2003, Pages 1528-1534

  Escudero, Tomas ^a,b   Abdelhadi, Iman ^a,c   Sandalinas, Mireia ^a,b   Munné, Santiago ^a,b  

^a SAINT BARNABAS MEDICAL CENTER   (United States)

^b Institute for Reproductive Medicine and Science   (United States)

^c Farah Hospital   (Jordan)

Author keywords

FISH; IVF; Miscarriage; PGD; Sperm; Translocation carriers

Indexed keywords

ARTICLE; BLOOD SAMPLING; CORRELATION ANALYSIS; EMBRYO; FEMALE; FERTILIZATION IN VITRO; FLUORESCENCE IN SITU HYBRIDIZATION; GAMETE; GENETIC PROCEDURES; HETEROZYGOTE; HUMAN; HUMAN CELL; IN SITU HYBRIDIZATION; LYMPHOCYTE; MALE; PREDICTION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RECIPROCAL CHROMOSOME TRANSLOCATION; SEMEN ANALYSIS;

EID: 0037497360     PISSN: 00150282     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0015-0282(03)00252-8     Document Type: Article

References (27)

1. Stern C., Pertile M., Norris H., Hale L., Baker H.W.G. Chromosome translocations in couples with in-vitro fertilization implantation failure. Hum Reprod. 14:1999;2097-2101.
2. Testart J., Gautier E., Brami C., Rolet F., Sedmon E., Thebault A. Intracytoplasmic sperm injection in infertile patients with structural chromosome abnormalities. Hum Reprod. 11:1996;2609-2612.
3. Meschede D., Lemcke B., Exeler J.R., De Geyter C., Behre H.M., Nieschlag E., et al. Chromosome abnormalities in 447 couples undergoing intracytoplasmatic sperm injection - prevalence, types, sex distribution and reproductive relevance. Hum Reprod. 13:1998;576-582.
4. Van der Ven K., Peschka B., Montag M., Lange R., Schwanitz G., van der Ven H.H. Increased frequency of congenital chromosomal aberrations in female partners of couples undergoing intracytoplasmic sperm injection. Hum Reprod. 13:1998;48-54.
5. Evsikov S., Cieslak M.L.T., Verlinsky Y. Effect of chromosomal translocations on the development of preimplantation human embryos in vitro. Fertil Steril. 74:2000;672-677.
6. Munné S., Scott R., Sable D., Cohen J. First pregnancies after preconception diagnosis of translocations of maternal origin. Fertil Steril. 69:1998;675-681.
7. Munné S., Morrison L., Fung J., Márquez C., Weier U., Bahĉe M., et al. Spontaneous abortions are reduced after preconception diagnosis of translocations. J Assist Reprod Genet. 15:1998;290-296.
8. Munné S., Fung J., Cassel M.J., Márquez C., Weier H.U.G. Preimplantation genetic analysis of translocations case-specific probes for interphase cell analysis . Hum Genet. 102:1998;663-674.
9. Munné S., Bahĉe M., Schimmel T., Sadowy S., Cohen J. Case report chromatid exchange and predivision of chromatids as other sources of abnormal oocytes detected by preimplantation genetic diagnosis of translocations . Prenat Diagn. 18:1998;1450-1458.
10. Conn C.M., Harper J.C., Winston R.M.L., Delhanty J.D.A. Infertility couples with Robertsonian translocations preimplantation genetic analysis of embryos reveals chaotic cleavage divisions . Hum Genet. 102:1998;117-123.
11. Verlinsky Y., Evsikov S. Karyotyping of human oocytes by chromosomal analysis of the second polar body. Mol Hum Reprod. 5:1999;89-95.
12. Willadsen S., Levron J., Munné S., Schimmel T., Márquez C., Scott R., et al. Rapid visualization of metaphase chromosomes in single human blastomeres after fusion with in vitro matured bovine eggs. Hum Reprod. 2:1999;470-475.
13. Munné S., Sandalinas M., Escudero T., Fung J., Gianaroli L., Cohen J. Outcome of preimplantation genetic diagnosis of translocations. Fertil Steril. 73:2000;1209-1218.
14. Munné S., Escudero T., Sandalinas M., Sable D., Cohen J. Gamete segregation in female carriers of Robertsonian translocations. Cytogenet Cell Genet. 90:2000;303-308.
15. Wyrobek A.J., Alhborn T., Balhorn R., Stanker L. Fluorescence in situ hybridization to Y chromosomes in decondensed human sperm nuclei. Mol Reprod Dev. 27:1990;200-208.
16. Bischoff F.Z., Nguyen D.D., Burt K.J., Shaffer L.G. Estimates of aneuploidy using multicolor fluorescence in situ hybridization on human sperm. Cytogenet Cell Genet. 66:1994;237-243.
17. Blanco J., Egozcue J., Clusellas N., Vidal F. FISH on sperm heads allows the analysis chromosome segregation and interchromosomal effects in carriers of structural rearrangements results in a translocation carrier, t(5;8)(q33;q13) . Cytogent Cell Genet. 83:1998;275-280.
18. Blanco J., Egozcue J., Vidal F. Incidence of chromosome 21 disomy in human spermatozoa as determined by fluorescent in-situ hybridization. Hum Reprod. 11:1996;722-726.
19. Jalbert P., Sèle B., Jalbert H. Reciprocal translocations a way to predict the mode of imbalanced segregation by pachytene-diagram drawing . Hum Genet. 55:1980;209-222.
20. Smith A., Gaha T.J. Data on families of chromosome translocation carriers ascertained because of habitual spontaneous abortion. Aust NZ J Obstet Gynaecol. 30:1990;57-62.
21. Midro A.T. Genetic counseling in the case of carrier state with reciprocal chromosome translocations. Wiad Lek. 45:1992;775-780. [In Polish].
22. Escudero T., Lee M., Sandalinas S., Munné S. Female gamete segregation in two carriers of translocations involving 2q and 14q. Prenat Diagn. 20:2000;235-237.
23. Van Assche E., Staessen C., Vegetti W., Bonduelle M., Vandervorst M., Van Steirteghem A., et al. Preimplantation genetic diagnosis and sperm analysis by fluorescence in-situ hybridization for the most common reciprocal translocation t(11;22). Mol Hum Reprod. 5:1999;682-690.
24. Munné S., Alikani M., Tomkin G., Grifo J., Cohen J. Embryo morphology, developmental rates and maternal age are correlated with chromosome abnormalities. Fertil Steril. 64:1995;382-391.
25. Harper J.K., Coonen E., Handyside A.H., Winston R.M.L., Hopman A.H., Delhanty J.D.A. Mosaicism of autosomes and sex chromosomes in morphologically normal, monospermic preimplantation human embryos. Prenat Diagn. 15:1995;41-49.
26. Munné S., Cohen J. Chromosome abnormalities in human embryos. Hum Reprod Update. 4:1998;842-855.
27. Escudero T., Lee M., Carrel D., Blanco J., Munné S. Analysis of chromosome abnormalities in sperm and embryos from two 45,XY,t(13;14)(q10;q10) carriers. Prenat Diagn. 20:2000;599-602.