Informace o publikaci

Sperm and embryo analysis of similar t(7;10) translocations transmitted in two families

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VOZDOVÁ Miluše ORÁČOVÁ Eva MUSILOVÁ Petra KAŠÍKOVÁ Kateřina PŘINOSILOVÁ Petra GAILLYOVÁ Renata RUBEŠ Jiří

Rok publikování 2011
Druh Článek v odborném periodiku
Časopis / Zdroj Fertility and Sterility
Fakulta / Pracoviště MU

Lékařská fakulta

Citace
Doi http://dx.doi.org/10.1016/j.fertnstert.2011.04.042
Obor Gynekologie a porodnictví
Klíčová slova Embryo; FISH; interchromosomal effect; meiotic segregation; reciprocal translocation; sperm
Popis Objective: To compare the sperm meiotic segregation profiles in two men from families with similar t(7;10) translocations and determine the frequency of unbalanced sperm and preimplantation embryos in one couple. Design: Analysis of sperm nuclei and blastomeres by fluorescence in situ hybridization (FISH). Setting: Research institute. Patient(s): Carriers of balanced translocations t(7;10)(q34;q24) and t(7; 10)(q36;q24.3). Intervention(s): Multicolor FISH using probes for chromosomes 7, 10, 8, 18, 21, X, and Y on sperm and preimplantation genetic diagnosis (PGD) of blastomeres. Main Outcome Measure(s): Frequencies of meiotic segregation products in sperm and blastomeres and sperm aneuploidy of chromosomes 8, 18, 21, X, and Y. Result(s): Similar meiotic segregation patterns, with preferential alternate segregation (50.6% in patient P1, 48.1% in P2) followed by adjacent 1, adjacent 2 and 3:1 segregations, were observed in the sperm of the two carriers. An interchromosomal effect on the sex chromosomes was found when compared with disomy frequencies reported in control donors. The results of preimplantation genetic diagnosis in the first couple are roughly consistent with the sperm analysis results. Conclusion(s): Carriers of similar translocations show similar segregation profiles. The in vitro fertilization method accompanied by preimplantation genetic diagnosis increases the chance of translocation carriers fathering a healthy child.

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