Carrier screening is a genetic test that determines if an individual carries a gene mutation that could lead to a genetic disorder if passed to their children. It’s crucial for couples planning to conceive, as it assesses the risk of transmitting genetic conditions. Carrier screening is available for various genetic disorders, including those prevalent in specific ethnic groups.

Diagnostic Benefits:

• Comprehensive Detection: Identifies a wide range of genetic conditions, including rare ones, with expanded panels.
• Informed Decision-Making: Helps couples make informed family planning choices, including IVF with PGD.
• Ethnic-Specific Screening: Tailored panels for conditions common in specific ethnic groups.
• High Sensitivity and Specificity: Ensures accurate and reliable results.
• Preconception Planning: Recommended for couples, particularly those with a higher risk of certain genetic disorders.
• Prenatal Care: Assesses fetal risk during pregnancy, with further testing if both parents are carriers.
• Family History: Useful for those with a family history of genetic disorders.