It is true that prenatal screening can be used to rule out all possible fetal abnormalities, because prenatal screening include prenatal cell-free DNA screening, blood tests, and a particular kind of ultrasound.
Many birth defects, including those that are genetic illnesses, can be detected during prenatal screening tests to determine if your kid is more or less likely to have them. These examinations include prenatal cell-free DNA screening, blood tests, and a particular kind of ultrasound.
The first or second trimester is typically when prenatal screening tests are available. Screening exams cannot provide a firm diagnosis. Your doctor will go over your options for a diagnostic test to confirm the diagnosis if the results show an elevated risk for a genetic condition.
You might think about an invasive prenatal diagnostic test if a screening test reveals a potential issue or if your age, family history, or medical history puts you at elevated risk of delivering a baby with a genetic condition.
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