To select cytogenetically normal embryos, preimplantation genetic diagnosis (PGD) aneuploidy screening (AS) is used in numerous centers around the world. Chromosomal abnormalities lead to developmental problems, implantation failure, and early abortion of embryos. The usefulness of PGD in identifying single-gene diseases, human leukocyte antigen typing, X-linked diseases, and specific genetic diseases is well-known. In this review, preimplantation embryo genetics, PGD research studies, and the European Society of Human Reproduction and Embryology PGD Consortium studies and reports are examined. In addition, criteria for embryo selection, technical aspects of PGD-AS, and potential noninvasive embryo selection methods are described. Indications for PGD and possible causes of discordant PGD results between the centers are discussed. The limitations of fluorescence in situ hybridization, and the advantages of the array comparative genomic hybridization are included in this review. Although PGD-AS for patients of advanced maternal age has been shown to improve in vitro fertilization outcomes in some studies, to our knowledge, there is not sufficient evidence to use advanced maternal age as the sole indication for PGD-AS. PGD-AS might be harmful and may not increase the success rates of in vitro fertilization. At the same time PGD, is not recommended for recurrent implantation failure and unexplained recurrent pregnancy loss. Copyright (C) 2014, Kaohsiung Medical University. Published by Elsevier Taiwan LLC. All rights reserved.
C1 [Sahin, Levent] Pk Hosp, Dept IVF, Malatya, Turkey.
[Bozkurt, Murat] Kafkas Univ, Fac Med, Dept Obstet & Gynecol, TR-36000 Kars, Turkey.
[Sahin, Hilal] Inonu Univ, Inonu Sch Med, Dept Histol & Embryol, Malatya, Turkey.
[Gurel, Aykut] HRS IVF & Genet Diag Ctr, Ankara, Turkey.
[Yumru, Ayse Ender] Taksim Educ & Res Hosp, Dept Obstet & Gynecol, Istanbul, Turkey.