Preimplantation genetic diagnosis for Down syndrome pregnancy.
- Author:
Yu ZHANG
1
;
Chen-ming XU
;
Yi-min ZHU
;
Min-yue DONG
;
Yu-li QIAN
;
Fan JIN
;
He-feng HUANG
Author Information
- Publication Type:Case Reports
- MeSH: Adult; Chromosomes, Human, Pair 21; genetics; Down Syndrome; diagnosis; genetics; Female; Humans; In Situ Hybridization, Fluorescence; Male; Monosomy; Pregnancy; Preimplantation Diagnosis
- From: Journal of Zhejiang University. Science. B 2007;8(7):515-521
- CountryChina
- Language:English
-
Abstract:
OBJECTIVETo evaluate the effect of preimplantation genetic diagnosis (PGD) conducted for women who had Down syndrome pregnancy previously.
METHODSTrisomy 21 was diagnosed by using fluorescence in site hybridization (FISH) before embryo transfer in two women who had Down syndrome pregnancies. Each received one or two PGD cycles respectively.
RESULTSCase 1: one PGD cycle was conducted, two oocytes were fertilized and biopsied. One embryo is of trisomy 21 and the other of monosomy 21. No embryo was transferred. Case 2: two PGD cycles were conducted, in total, sixteen oocytes were fertilized and biopsied. Four embryos were tested to be normal, six of trisomy 21, and one of monosomy 21. Five had no signal. Four normal embryos were transferred but no pregnancy resulted.
CONCLUSIONFor couples who had pregnancies with Down syndrome previously, PGD can be considered, and has been shown to be an effective strategy.