About The PGD/PGS
An Overview of Preimplantation Genetic Diagnosis (PGD) and Preimplantation Genetic Screening (PGS)
What is PGD?
Preimplantation Genetic Diagnosis (PGD) is a valuable technique that allows us to screen embryos for genetic disorders, significantly reducing the risk of passing on inherited diseases to offspring. Among the conditions we can screen for are Cystic Fibrosis, X Chromosome Fragility, Myotonic Dystrophy, and Thalassemia.
PGD is typically integrated into in vitro fertilization (IVF) programs. It can assist parents in selecting the sex of their baby, balancing the genders of their family members, or fulfilling specific gender preferences.
Our experienced medical team uses advanced microscopy to evaluate the early embryos created during IVF, enabling them to determine the gender before transferring the embryos into the mother’s uterus. This process allows us to select only the desired gender for implantation.
When is PGD Indicated?
- Abnormal chromosome numbers
- Sex selection
- Genetic mutations
- History of recurrent miscarriages
- A family history of chromosomal abnormalities
- Preventing the transmission of diseases to offspring
What is PGS?
Preimplantation Genetic Screening (PGS) also employs PGD technology to enhance the likelihood of a successful pregnancy for women who have faced multiple miscarriages or infertility struggles. This screening involves assessing the chromosomes for abnormalities (aneuploidy) to ensure the proper development of the embryo prior to uterine transfer.
Our physicians will tailor the best treatment plan to meet each client’s individual needs, aiming for optimal outcomes. PGS has proven effective, helping many mothers successfully conceive healthy babies.
When is PGS Indicated?
- History of unsuccessful IVF treatments
- Women aged over 35
- Family history of chromosomal abnormalities
- Experience of multiple miscarriages
Understanding the Risks of PGD and PGS
Both PGD and PGS are considered low-risk procedures, performed by our skilled medical professionals. However, like any medical intervention, they come with certain risks. We will discuss the success rates and any potential risks of the treatment with you prior to starting to ensure you are fully informed.
It’s important to note that embryos may have chromosomal inconsistencies from cell to cell, leading to potential false negative or false positive results. These discrepancies can occasionally impact the accuracy of the treatment or the success of the IVF process.
We want to assure you that even in the event of such complications, we will remain dedicated to supporting you throughout the journey and will do our utmost to help you achieve your dream of parenthood.
