Sperm chromosome analysis of two males heterozygous for a t(2;17)(q35;p13) and t(3;8)(p13;p21) reciprocal translocation
- PMID: 1427772
- DOI: 10.1007/BF00210768
Sperm chromosome analysis of two males heterozygous for a t(2;17)(q35;p13) and t(3;8)(p13;p21) reciprocal translocation
Abstract
Sperm chromosome complements from two males, one heterozygous for the reciprocal translocation t(2;17)(q35;p13) (n = 18) and one for t(3;8) (p13;p21) (n = 73), were analyzed. Only 2:2 segregations were observed with t(2;17): alternate, 56%; adjacent-I, 33%; adjacent-II, 11%. Both 2:2 and 3:1 meiotic segregations occurred in t(3;8): alternate, 34.2%; adjacent-I, 43.8%; adjacent-II, 20.5% and 3:1, 1.4%. A significant excess of chromosomally normal versus balanced sperm complements was observed with both translocation heterozygotes. The frequencies of other chromosome aberrations unrelated to the translocations were 16.7% for t(2;17) and 8.2% for t(3;8). The ratio of X-bearing to Y-bearing sperm was not different from the theoretically expected ratio of 1:1.
Similar articles
-
Segregation analysis of four translocations, t(2;18), t(3;15), t(5;7), and t(10;12), by sperm chromosome studies and a review of the literature.Cytogenet Cell Genet. 1995;70(1-2):80-7. doi: 10.1159/000133997. Cytogenet Cell Genet. 1995. PMID: 7736796 Review.
-
Sperm chromosome analysis of two men heterozygous for reciprocal translocations: t(1;9)(q22;q31) and t(16;19)(q11.1;q13.3).Cytogenet Cell Genet. 1992;60(1):18-21. doi: 10.1159/000133285. Cytogenet Cell Genet. 1992. PMID: 1582252
-
Chromosome complements in 695 sperm from three men heterozygous for reciprocal translocations, and a review of the literature.Hereditas. 1993;118(2):165-75. doi: 10.1111/j.1601-5223.1993.00165.x. Hereditas. 1993. PMID: 8335473
-
Sperm chromosome complements in a man heterozygous for a reciprocal translocation t(2;3)(q24;p26).Hum Reprod. 1994 Aug;9(8):1512-5. doi: 10.1093/oxfordjournals.humrep.a138739. Hum Reprod. 1994. PMID: 7989514
-
Sperm chromosome complements in a man heterozygous for a reciprocal translocation 46,XY,t(9;13)(q21.1;q21.2) and a review of the literature.Clin Genet. 1995 Jan;47(1):42-6. doi: 10.1111/j.1399-0004.1995.tb03920.x. Clin Genet. 1995. PMID: 7774043 Review.
Cited by
-
Clinical features of carriers of reciprocal chromosomal translocations involving chromosome 2: report of nine cases and review of the literature.Int Braz J Urol. 2018 Jul-Aug;44(4):785-793. doi: 10.1590/S1677-5538.IBJU.2017.0233. Int Braz J Urol. 2018. PMID: 29219278 Free PMC article. Review.
-
Fertility problems in men carrying a translocation involved in breakpoints on chromosome 17p13: A retrospective, observational study.Medicine (Baltimore). 2022 Dec 9;101(49):e32216. doi: 10.1097/MD.0000000000032216. Medicine (Baltimore). 2022. PMID: 36626513 Free PMC article.