Ensuring fetal health is a top priority for expectant mothers, and prenatal screening tests play a crucial role in monitoring the baby’s well-being. One such test is amniocentesis, a diagnostic procedure used to detect potential genetic disorders in the fetus. Here’s what you need to know about this test.
Amniocentesis is a prenatal diagnostic test typically performed during the second trimester (between weeks 15 and 21 of pregnancy). Since it is an invasive procedure, it is only recommended in specific cases, such as:
The test analyzes amniotic fluid, which contains fetal cells, providing valuable insights into the baby’s health, including:
✅ Diagnosis of Fetal Infections – Detects infections that may impact fetal development.
✅ Fetal Lung Maturity – Assesses whether the baby’s lungs are developed enough for birth.
✅ Genetic Testing – Identifies chromosomal or genetic disorders that could cause intellectual or physical disabilities.
The procedure follows several carefully controlled steps:
The entire process typically takes 20-30 minutes and does not require anesthesia.
Although amniocentesis is generally safe, it does carry some risks:
Due to its invasive nature, amniocentesis is not routinely performed for all pregnancies but is recommended only in cases with specific medical indications.
If you have concerns about fetal health or are considering amniocentesis, contact Sakalli IVF today. Our experienced team is here to provide expert guidance and support, helping you make informed decisions about your pregnancy journey.
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