What Is Amniocentesis?

Amniocentesis is an advanced prenatal test that helps detect genetic or chromosomal abnormalities in the developing baby. During the test, a small amount of amniotic fluid is taken from the uterus and examined in a laboratory. The fluid contains the baby’s cells and important chemicals that provide valuable information about genetic health.

When Is Amniocentesis Recommended?

Doctors recommend amniocentesis when screening tests show an increased risk of genetic disorders such as Down syndrome, thalassemia, or neural tube defects. It is also advised for women over 35 years, those with abnormal ultrasound findings, or a family history of inherited conditions. At Isha IVF Centre in Palanpur, this procedure is performed only when medically necessary and after detailed counseling.

How Is the Procedure Performed?

The test is usually done between 15 and 20 weeks of pregnancy. Using ultrasound guidance, a thin needle is carefully inserted into the uterus to collect a small amount of amniotic fluid. The process takes only a few minutes and is performed with utmost care to ensure safety for both mother and baby.

Benefits of Amniocentesis

Amniocentesis offers accurate results that help parents make informed decisions about their pregnancy. It can detect chromosomal abnormalities, genetic conditions, and even infections. Early diagnosis allows doctors to plan appropriate management and ensures better outcomes for the baby’s health.