Preconception Carrier Screening

Carrier screening helps determine whether you or your partner carry genetic variants associated with inherited disorders such as:

• Cystic Fibrosis (CF)
• Spinal Muscular Atrophy (SMA)
• Other inherited genetic conditions

This information can help couples understand potential risks before planning a pregnancy.

Preimplantation Genetic Testing (PGT)

For couples undergoing IVF treatment, PGT evaluates embryos for chromosomal abnormalities and specific genetic disorders before implantation.

Benefits include:

• Improved embryo selection
• Reduced risk of inherited genetic conditions
• Enhanced IVF success rates

Non-Invasive Prenatal Testing (NIPT)

NIPT is a simple blood test that analyzes fetal DNA circulating in the mother's blood. It can screen for common chromosomal conditions, including:

• Down Syndrome (Trisomy 21)
• Trisomy 18
• Trisomy 13

Testing can typically be performed from 9–10 weeks of pregnancy.

Genomic Infertility Diagnostics

Advanced genomic analysis helps identify genetic and microbial factors that may contribute to:

• Male infertility
• Female infertility
• Recurrent pregnancy loss
• Implantation failure
• Endometrial receptivity issues