Services
Ultrasound Scans
Ultrasound scans use high-frequency sound waves to create images of the inside of the body. They're commonly used in prenatal care, diagnosing conditions, and guiding procedures. Non-invasive and safe, ultrasounds provide real-time imaging, aiding in the assessment of organs, tissues, and blood flow without radiation exposure.
High Risk Pregnacy Scan
A high-risk pregnancy scan involves detailed ultrasound examinations to monitor the health and development of the fetus and the mother. These scans, performed more frequently, help detect potential complications such as fetal growth restrictions, placental issues, or congenital abnormalities. They guide early interventions, ensuring better outcomes for both mother and baby.
Genetic Counseling
Genetic counseling is a process where individuals or families receive guidance and information about genetic conditions. It involves evaluating family history, discussing the risks of inherited disorders, and interpreting genetic test results. Counselors help patients understand their options, make informed decisions, and manage any potential health implications, ensuring personalized and compassionate care.
Nipt Test
The Non-Invasive Prenatal Test (NIPT) is a screening method used during pregnancy to detect certain genetic conditions in the fetus, such as Down syndrome, trisomy 18, and trisomy 13. It analyzes small fragments of fetal DNA circulating in the mother's blood, offering high accuracy with minimal risk compared to invasive procedures like amniocentesis.
CVS Sampling
Chorionic Villus Sampling (CVS) is a prenatal test that involves taking a small sample of placental tissue (chorionic villi) to test for genetic abnormalities in the fetus. Typically performed between the 10th and 13th weeks of pregnancy, CVS can diagnose conditions like Down syndrome and cystic fibrosis. The procedure carries a small risk of complications, but it provides early and accurate genetic information.
Amniocentesis
Amniocentesis is a prenatal diagnostic procedure in which a small amount of amniotic fluid is extracted from the uterus using a needle. Typically performed between the 15th and 20th weeks of pregnancy, it tests for genetic abnormalities, neural tube defects, and fetal infections. While highly accurate, the procedure carries a small risk of complications such as miscarriage.
