Screening for Genetic Anomalies in Fetus

Advanced Fetal Genetic Screening

• Non-Invasive Prenatal Testing (NIPT): A highly accurate blood test that screens for common genetic conditions, such as Down syndrome, trisomy 18, and trisomy 13, by analyzing fetal DNA found in the mother’s blood. This test is performed early in pregnancy and has a low risk of false positives.
• First Trimester Screening: Combines a blood test and an early ultrasound to assess the risk of chromosomal abnormalities, including Down syndrome. This screening typically includes measuring the nuchal translucency (fluid at the back of the baby’s neck) via ultrasound.
• Second Trimester Screening: Includes the quad screen or multiple marker test, which measures levels of specific substances in the mother’s blood to evaluate the risk of certain genetic disorders and neural tube defects.

Expert Care Team

• Specialized Obstetricians and Geneticists: Access to experienced professionals who provide detailed evaluations, interpret screening results, and offer guidance on next steps.
• Multidisciplinary Approach: Collaboration with genetic counselors, sonographers, and other healthcare professionals to ensure comprehensive care and accurate results.
• Continuous Education: Commitment to using the latest advancements and research in genetic screening to offer the most effective and up-to-date services.

Supportive and Compassionate Care

• Personalized Counseling: One-on-one consultations to explain screening processes, discuss results, and address any concerns or questions about potential genetic anomalies and their implications.
• Emotional Support: Access to counseling services to help manage the emotional and psychological aspects of genetic screening and the possibility of identifying anomalies.
• Patient Education: Detailed information about genetic screening options, potential findings, and what to expect, ensuring you are well-informed and prepared for each stage of the screening process.

Holistic Health and Follow-Up

• Lifestyle and Wellness Guidance: Recommendations on maintaining overall health and wellness to support a healthy pregnancy and ensure the best outcomes from genetic screening.
• Regular Monitoring: Follow-up appointments to review screening results, discuss additional testing if needed, and provide ongoing support and care.
• Long-Term Planning: Ongoing assistance to address any long-term considerations related to fetal genetic anomalies and family planning, ensuring continued support and informed decision-making.