It is a diagnostic technique to check for genetic abnormalities in unborn babies. The test involves taking a sample of the amniotic fluid which surrounds the growing baby inside the womb. It is usually done about the 16th week of pregnancy as by this stage there is enough amniotic fluid to allow the test to be carried out and enough time to terminate the pregnancy in case genetic abnormalities are detected. This can help prevent later suffering of the baby and the family.
For obtaining a sample a hollow needle is carefully inserted under local anaesthesia through the expectant mother’s abdomen. The amount of fluid withdrawn is only about 20 ml. This fluid contains cells from the developing baby. Chemical and microscopic examinations of these cells can provide invaluable information, revealing the presence or absence of genetic disorders which cannot be detected otherwise.
The chromosome analysis of the cells in the amniotic fluid can also reveal the sex of the baby.