Preimplantation Genetic Diagnosis (PGD) in North Cyprus
What Is PGD?
PGD (Preimplantation Genetic Diagnosis) is a genetic testing method used during IVF treatment to identify embryos that are free from certain inherited diseases before embryo transfer.
During PGD testing, embryos created in the laboratory are genetically analyzed to detect chromosomal abnormalities or specific genetic disorders. By selecting embryos with a normal genetic structure, fertility specialists can improve the chances of achieving a healthy pregnancy.
This approach helps ensure that the embryo transferred during IVF has the highest potential for healthy development.
PGD in IVF Treatment
PGD in Cyprus has become an important part of modern IVF treatment because it allows fertility specialists to evaluate embryo genetics before transfer.
Main advantages of PGD include:
- Selecting genetically healthy embryos
- Increasing pregnancy success rates
- Reducing miscarriage risk
- Preventing inherited genetic diseases
- Improving overall IVF treatment outcomes
By transferring embryos with normal genetic results, the IVF process can become more effective and emotionally less stressful for patients.
How Is PGD Testing Performed?
PGD testing is recommended only when medically necessary. The process usually includes several steps during IVF treatment.
Embryo Development
After fertilization during IVF treatment, embryos develop in the laboratory until they reach the blastocyst stage.
Embryo Biopsy
A small number of cells are carefully taken from the embryo. This procedure is performed by experienced embryologists and does not harm embryo development.
Genetic Analysis
The collected cells are sent to a specialized genetic laboratory where advanced testing is performed to evaluate the embryo’s genetic structure.
Embryo Selection
Based on the results, embryos with normal genetic profiles are selected for embryo transfer.
What Conditions Can PGD Detect?
PGD testing can identify many inherited diseases before pregnancy occurs.
Single Gene Disorders (PGD-M)
PGD-M is used when parents carry a specific genetic mutation that could be passed to the baby.
Examples include:
- Beta Thalassemia
- Sickle Cell Disease
- Spinal Muscular Atrophy (SMA)
- Cystic Fibrosis
- Congenital Hearing Loss
This testing helps prevent the transmission of inherited diseases.
Chromosomal Disorders (PGT-A)
Chromosomal screening can detect abnormalities such as:
- Down Syndrome
- Edwards Syndrome
- Patau Syndrome
- Turner Syndrome
- Klinefelter Syndrome
Screening embryos before transfer can significantly improve IVF success rates.
Who Should Consider PGD Testing?
PGD in Cyprus may be recommended for patients who:
- Are over the age of 35
- Have experienced repeated IVF failures
- Have a history of recurrent miscarriage
- Carry genetic diseases in the family
- Had abnormal chromosome results in previous pregnancies
A fertility specialist will determine whether PGD testing is appropriate after evaluating the patient’s medical history.
PGD Testing at Dogus IVF Center
At Dogus IVF Center, advanced genetic testing technologies are used as part of IVF treatment when medically necessary.
Our experienced embryology and genetics teams work together to analyze embryo health and select embryos with the highest implantation potential.
If you would like more information about PGD in Cyprus, our fertility specialists will be happy to guide you through the testing process and treatment options.
