AMNIOCENTESIS — SECOND-TRIMESTER GENETIC TESTING IN EXPERT HANDS
Amniocentesis is a specialised second-trimester diagnostic procedure that provides definitive genetic and chromosomal information through the analysis of amniotic fluid collected under real-time ultrasound guidance.
Amniocentesis is a highly accurate diagnostic procedure performed during the second trimester when specific genetic, chromosomal, or fetal concerns require definitive testing. Unlike screening tests, amniocentesis provides direct genetic information through analysis of amniotic fluid obtained under continuous ultrasound guidance.
At ADI Advanced Centre for Fetal Care, every amniocentesis procedure is performed personally by a fetal medicine specialist using real-time ultrasound guidance and internationally accepted safety protocols. Our approach combines procedural expertise, comprehensive counselling, and careful follow-up so families receive accurate answers, clear guidance, and confident support throughout the process.
Whether recommended following abnormal screening results, ultrasound findings, genetic concerns, or maternal age-related risk factors, every procedure is conducted with the precision expected from a dedicated fetal medicine centre.
Amniocentesis is a specialised invasive procedure requiring advanced ultrasound skills, procedural precision, and comprehensive patient counselling. The quality and safety of the procedure depend significantly on specialist expertise and adherence to established fetal medicine protocols.
At ADI Advanced Centre for Fetal Care, every amniocentesis is performed according to internationally recognised standards, ensuring families receive expert care, accurate diagnosis, and personalised support throughout their pregnancy journey.
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Provides highly accurate chromosomal and genetic information when screening tests indicate an increased risk.
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Performed under continuous ultrasound visualisation to ensure precise needle placement and procedural safety.
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Can diagnose conditions such as Down syndrome, Edwards syndrome, Patau syndrome, and other chromosomal disorders.
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Often recommended when fetal anomalies or soft markers are identified during pregnancy scans.
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Allows advanced laboratory testing, including chromosome analysis and specialised genetic investigations when clinically indicated.
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Detailed discussion of indications, benefits, risks, limitations, and results interpretation is provided at every stage.
FREQUENTLY ASKED QUESTIONS
Amniocentesis is a diagnostic procedure in which a small sample of amniotic fluid is collected for genetic, chromosomal, or other specialised laboratory testing.
The procedure is most commonly performed between 15 and 22 weeks of pregnancy, depending on the clinical indication.
It may be recommended following abnormal screening results, concerning ultrasound findings, family history of genetic conditions, advanced maternal age, or previous affected pregnancies.
No. Amniocentesis is a diagnostic test that can provide definitive genetic and chromosomal information for many conditions.
The procedure itself usually takes only a few minutes, although the complete appointment may take 30–60 minutes including counselling and observation.
Most patients experience mild discomfort similar to a blood test or brief cramping sensation. Significant pain is uncommon.
When will I receive my results?
Result timelines vary depending on the laboratory tests requested. Some preliminary results may be available within a few days, while comprehensive genetic testing can take longer.
