Gender Selection | Family Balancing | Genetic Testing (PGS)
Gender Selection and Genetic screening before implantation of the embryo: Once IVF/ICSI has been performed, we will carry out genetic testing on embryos in order to avoid any chromosomal abnormalities and you can also choose the gender of your baby if there is a preference. We have Three options for genetic testing: FISH – Standard NGS – High-Resolution NGS
one embryo NGS Testing | 4,000 AED Per Embryo
Embryo Diagnosis for one embryo only using the Next-generation Sequencing (NGS) method allows for the screening of the most common chromosomal abnormalities caused by aneuploidy, missing, or additional whole chromosomes, in chromosomes 13, 18, 21 (Down syndrome), X & Y.
5-Chromosome Aneuploidy Screening – FISH | 8,000 AED
Embryo screening using the FISH method allows for the screening of the most common chromosomal abnormalities caused by aneuploidy, missing or additional whole chromosomes, in chromosomes 13, 18, 21 (Down syndrome), X and Y.
Embryo Screening by Standard Resolution Next Generation Sequencing | 13,900 AED
Next Generation Sequencing is used for embryo screening for all 24 Chromosomes for detection of aneuploidy, missing or additional chromosomes & Gender Detection
Embryo Screening by High-Resolution Next Generation Sequencing | 18,000 AED
High-Resolution Next Generation Sequencing is a breakthrough in embryo screening that allows for the following six tests to be completed one test at one time:
1. 24-chromosome aneuploidy screening
2. Identification of a Single Gene Disorder (PGD Single Gene Disorder)
3. Translocation/Inversion detection
4. Microdeletion detection down to 2Mbase
5. Gender identification
6. Direct HLA matching
