Amniocentesis is a prenatal diagnostic test for detecting certain genetic and chromosomal conditions. At Garbh, it is performed with ultrasound guidance and expert fetal medicine care.
An amniocentesis test involves collecting a small sample of amniotic fluid surrounding the baby. The sample contains fetal cells that can be examined for certain chromosomal and genetic conditions. Unlike screening tests that estimate the possibility of a condition, amniocentesis can provide diagnostic information. It may be recommended when previous screening, ultrasound findings, or family history indicates an increased risk.
Amniocentesis may be recommended when there is a higher risk of a genetic or chromosomal condition. It is generally performed between 15 and 20 weeks of pregnancy, depending on your medical needs.
It may be considered when:
Before the procedure, the specialist reviews your reports and explains the benefits, limitations, risks, and appropriate timing.
Garbh offers specialised fetal medicine care for families who need an amniocentesis test in Chandigarh. The team focuses on proper evaluation, ultrasound-guided procedures, and clear counselling to help you make informed decisions about prenatal testing.
Amniocentesis is an invasive procedure, so it has some potential risks. Although serious complications are uncommon, it is important to understand these risks before making a decision.
Possible complications can include:
The procedure should only be undertaken when medically appropriate and after discussing the potential benefits and risks with a qualified specialist. Garbh follows ultrasound-guided protocols and provides counselling before the procedure.