Monopaternal superfecundation of quintuplets after transfer of two embryos in an in vitro fertilization cycle

被引:6
作者
Amsalem, H
Tsvieli, R
Zentner, BS
Yagel, S
Mitrani-Rosenbaum, S
Hurwitz, A
机构
[1] Hadassah Univ Hosp, Dept Obstet & Gynecol, IVF Div, IL-91120 Jerusalem, Israel
[2] Hadassah Univ Hosp, Unit Dev Mol Biol & Genet Engn, IL-91120 Jerusalem, Israel
关键词
superfecundation; fetal reduction; IVF; genetic analysis;
D O I
10.1016/S0015-0282(01)01976-8
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To present the first genetically proven identity of quintuplets in an IVF treatment cycle after transferring only two embryos. Design: Case report. Setting: IVF unit and obstetrics department of university-affiliated general hospital. Patient(s): Twenty-five-year-old patient undergoing IVF treatment for unexplained infertility. Intervention(s): In vitro fertilization with intracytoplasmic sperm injection performed on 50% of oocytes, resulting in successful production of nine early-cleavage embryos. Transfer of two embryos on day 3 and freezing of the remaining embryos. Main Outcome Measure(s): Development of five separate embryonic sacs. Fetal reduction of three embryos at 12 weeks of gestation. Result(s): Successful completion of the twin pregnancy and full genetic analysis of the three embryos and the twins that were born at term. Conclusion(s): Despite transferring only two embryos, superfecundation occurred, resulting in five embryos. Genetic analysis can be used to determine paternity and identity of all the embryos. (Fertil Steril(R) 2001;76: 621-3. (C) 2001 by American Society for Reproductive Medicine).
引用
收藏
页码:621 / 623
页数:3
相关论文
共 6 条
[1]   Time interval from human chorionic gonadotrophin (HCG) injection to follicular rupture [J].
Andersen, AG ;
AlsNielsen, B ;
Hornnes, PJ ;
Andersen, LF .
HUMAN REPRODUCTION, 1995, 10 (12) :3202-3205
[2]  
FISCHER RA, 1993, FERTIL STERIL, V60, P418
[3]  
Harris D W, 1982, J Reprod Med, V27, P39
[4]  
James W. H., 1993, Acta Geneticae Medicae et Gemellologiae, V42, P257
[5]   Hereditary inclusion body myopathy maps to chromosome 9p1-q1 [J].
MitraniRosenbaum, S ;
Argov, Z ;
Blumenfeld, A ;
Seidman, CE ;
Seidman, JG .
HUMAN MOLECULAR GENETICS, 1996, 5 (01) :159-163
[6]  
Wenk R E, 1991, Transfus Med, V1, P253, DOI 10.1111/j.1365-3148.1991.tb00041.x