Amniocentesis is a prenatal diagnostic test that involves the extraction of a small amount of amniotic fluid from the amniotic sac surrounding the fetus. This fluid contains fetal cells and other substances that can be analyzed for various purposes.
1. Biochemical abnormalities in the fetus: Amniotic fluid can be tested for specific substances, such as alpha-fetoprotein (AFP), which can indicate certain fetal abnormalities like neural tube defects or kidney problems.
2. Errors of metabolism in the fetus: Amniotic fluid can also be used to test for specific metabolic disorders, such as phenylketonuria (PKU) or cystic fibrosis, by evaluating enzyme levels or other metabolic markers.
3. Chromosomal abnormalities in the fetus: The fetal cells present in the amniotic fluid can be used to perform chromosomal analysis, such as karyotyping or fluorescence in situ hybridization (FISH), to detect conditions like Down syndrome, trisomy 18, or other chromosomal abnormalities.
In summary, amniocentesis is a valuable prenatal diagnostic tool that can provide information about a variety of potential abnormalities in a developing fetus, including biochemical, metabolic, and chromosomal issues.