What are Fetal Genetic Screening Tests? Fetal genetic screening tests are tests performed during pregnancy to evaluate the baby's genetic structure and identify possible genetic disorders. These tests are important for the health of the expectant mother and the baby.

Types of Fetal Genetic Screening Tests:

1. Ultrasonography (USG): It is used to monitor the baby's development and identify possible structural anomalies.
2. Dual Screening Test: Through a combination of blood tests and ultrasonography, it assesses the possibility of Down syndrome and other genetic disorders in the baby.
3. Triple and Quadruple Screening Tests: It assesses the baby's risk by measuring levels of certain proteins and hormones in the mother's blood.
4. Noninvasive Prenatal Testing (NIPT): By analyzing the baby's DNA from the mother's blood, genetic disorders are detected.

Purpose of Fetal Genetic Screening Tests:

• Monitoring the healthy development of the baby.
• To inform the expectant mother about possible risks.
• Referral to further diagnostic tests if necessary.

Fetal Genetic Screening Tests and Pregnancy Follow-up: Fetal genetic screening tests are an important part of pregnancy follow-up. These tests help the expectant mother to better manage the pregnancy process and provide early intervention when necessary.