Chromosome abnormalities in one thousand infertile males with nonobstructive sperm disorders

Fertility and Sterility

Volumn 86, Issue 6, 2006, Pages 1792-1795

  Elghezal, Hatem ^a   Hidar, Samir ^a   Braham, Rim ^a   Denguezli, Walid ^b   Ajina, Mounir ^a   Saâd, Ali ^a  

^a FARHAT HACHED HOSPITAL   (Tunisia)

^b FATTOUMA BOURGUIBA UNIVERSITY HOSPITAL   (Tunisia)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME ABERRATION; CYTOGENETICS; FLUORESCENCE IN SITU HYBRIDIZATION; GENE MUTATION; HUMAN; INFERTILITY; OLIGOSPERMIA; PRIORITY JOURNAL; SEX CHROMOSOME; SPERMATOGENESIS; SPERMATOZOON ABNORMALITY; TUNISIA;

AZOOSPERMIA; CHROMOSOME ABERRATIONS; HUMANS; INFERTILITY, MALE; MALE; PREVALENCE; RETROSPECTIVE STUDIES; RISK ASSESSMENT; RISK FACTORS; TUNISIA;

EID: 33751167216     PISSN: 00150282     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.fertnstert.2006.04.041     Document Type: Article

References (28)

1. Yoshida A., Miura K., and Shirai M. Cytogenetic survey of 1,007 infertile males. Urol Int 58 (1997) 166-176
2. Retief A.E., Van Zyl J.A., Menkveld R., Fox M.R., Kotze G.M., and Brusnicky J. Chromosome studies in 496 infertile males with a sperm count below 10 million/ml. Hum Genet 66 (1984) 162-164
3. Bourrouillou G., Dastugue N., and Colombies P. Chromosome studies in 925 infertile males with a sperm count below 10 million/ml. Hum Genet 71 (1985) 366-367
4. Van Assche E., Bonduelle M., Tournaye H., Joris H., Verheyen G., Devroey P., et al. Cytogenetics of infertile men. Hum Reprod 11 Suppl 4 (1996) 1-24
5. World Health Organization. WHO laboratory manual for the examination of human semen and semen-cervical mucus interaction. 4th ed (1999), Cambridge University Press, Cambridge
6. Mitelman F. ISCN 1995-an international system for human cytogenetic nomenclature (1995), S. Karger, Basel
7. Egozcue S., Blanco J., Vendrell J.M., Garcia F., Viga A., and Aran B. Human male infertility: chromosome anomalies, meiotic disorders, abnormal spermatozoa and recurrent abortion. Hum Reprod Update 6 (2000) 93-105
8. Tuerlings J.H., de France H.F., Hamers A., Hordijk R., Van Hemel J.O., Hansson K., et al. Chromosome studies in 1792 males prior to intra-cytoplasmic sperm injection: the Dutch experience. Eur J Hum Genet 6 (1998) 194-200
9. Nakamura Y., Kitamura M., Nishimura K., Koga M., Kondoh N., Takeyama M., et al. Chromosomal variants among 1790 infertile men. Int J Urol 8 (2001) 49-52
10. Nagvenkar P., Desai K., Hinduja I., and Zaveri K. Chromosomal studies in infertile men with oligozoospermia and non-obstructive azoospermia. Indian J Med Res 122 (2005) 34-42
11. Ismail S.R., el-Beheiry A.H., Hashishe M.M., and el-Bahaei M.E. Cytogenetic study in idiopathic infertile males. J Egypt Public Health Assoc 68 (1993) 179-204
12. Gunduz G., Luleci G., and Baykara M. Cytogenetic study in 102 infertile men. Urol Int 61 (1998) 32-34
13. Nielsen J., and Wohlert M. Chromosome abnormalities found among 34,910 newborn children: results from a 13-year incidence study in Århus, Denmark. Hum Genet 87 (1991) 81-83
14. Rives N., Joly G., Machy A., Simeon N., Leclerc P., and Mace B. 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
15. Blanco J., Egozcue J., and Vidal F. Meiotic behaviour of the sex chromosomes in three patients with sex chromosome anomalies (47,XXY, mosaic 46,XY/47,XXY and 47,XYY) assessed by fluorescence in-situ hybridisation. Hum Reprod 16 (2001) 887-892
16. Mroz K., Carrel L., and Hunt P.A. Germ cell development in the XXY mouse: evidence that X chromosome reactivation is independent of sexual differentiation. Dev Biol 207 (1999) 229-238
17. Shi Q., and Martin R.H. 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
18. Tuck-Muller C.M., Chen H., Martinez J.E., Shen C.C., Li S., Kusyk C., et al. Isodicentric Y chromosome, cytogenetic, molecular and clinical studies and review of the literature. Hum Genet 96 (1995) 119-129
19. Valetto A., Bertini V., Rapalini E., Baldinotti F., Di Martino D., and Simi P. Molecular and cytogenetic characterization of a structural rearrangement of the Y chromosome in an azoospermic man. Fertil Steril 8 (2004) 1388-1390
20. De Braekeleer M., and Dao T.N. Cytogenetic studies in male infertility: a review. Hum Reprod 6 (1991) 245-250
21. Baccetti B., Capitani S., Collodel G., Estenoz M., Gambera L., and Piomboni P. Infertile spermatozoa in a human carrier of Robertsonian translocation 14;22. Fertil Steril 78 (2002) 1127-1130
22. Rosenmann A., Wahrman J., Richler C., Voss R., Persitz A., and Goldman B. Meiotic association between the XY chromosomes and unpaired autosomal elements as a cause of human male sterility. Cytogenet Cell Genet 39 (1985) 19-29
23. Luciani J.M., Guichaoua M.R., Mattei A., and Morazzani M.R. Pachytene analysis of a man with a 13q;14q translocation and infertility. Cytogenet Cell Genet 38 (1984) 14-22
24. Pernice F., Mazza G., Puglisi D., Luppino M.G., and Frisina N. Nonrobertsonian translocation t(6;11) is associated with infertility in an oligoazoospermic male. Fertil Steril 78 (2002) 192-194
25. Chandley A.C. Genetic contribution to male infertility. Hum Reprod 13 Suppl 3 (1998) 76-83
26. Brown G.M., Leversha M., Hulten M., Ferguson-Smith M.A., Affara N.A., and Furlong R.A. Genetic analysis of meiotic recombination in humans by use of sperm typing: reduced recombination within a heterozygous paracentric inversion of chromosome 9q32-q34.3. Am J Hum Genet 62 (1998) 1484-1492
27. Ichioka K., Yoshimura K., Honda T., Takahashi A., and Terai A. Paracentric inversion of chromosome 7(q22-31) associated with nonobstructive azoospermia. Fertil Steril 83 (2005) 455-456
28. Anton E., Blanco J., Egozcue J., and Vidal F. Risk assessment and segregation analysis in a pericentric inversion inv6p23q25 carrier using FISH on decondensed sperm nuclei. Cytogenet Genome Res 97 (2002) 149-154