Amniocentesis
Amniocentesis is a specialized diagnostic procedure used during pregnancy to detect genetic disorders, chromosomal abnormalities, and certain fetal infections. Typically performed between 15 and 20 weeks of gestation, this test provides crucial information about the baby’s health and development.
During the procedure, a small amount of amniotic fluid (which surrounds the baby in the uterus) is safely collected using a thin needle under ultrasound guidance. This fluid contains fetal cells and important proteins that help in detecting conditions such as:
- Down syndrome
- Spina bifida
- Thalassemia and other inherited disorders
- Neural tube defects and infections
When is Amniocentesis Recommended?
- Abnormal results from other screening tests
- Family history of genetic disorders
- Previous child with a genetic condition
- Advanced maternal age (35 years or older)
Why Choose Us?
- Performed by experienced fetal medicine specialists
- Strict safety protocols and sterile technique
- Accurate results and post-test counseling
- Emotional support and professional guidance
At our center, we ensure that every amniocentesis procedure is conducted with precision, care, and compassion, helping parents make informed decisions about their pregnancy journey.
