What is testing a fetus for a genetic disorder called?

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Multiple Choice

What is testing a fetus for a genetic disorder called?

Explanation:
Foetal screening is the process of checking the fetus during pregnancy for potential genetic disorders. It aims to estimate the risk of a condition so parents can decide on further testing or management. Noninvasive methods, like analyzing fetal DNA in the mother's blood or using ultrasound markers, are common first steps. If a higher risk is detected, invasive tests such as amniocentesis can provide a definitive diagnosis. Prenatal screening is a closely related term, since prenatal means before birth, but foetal screening specifically emphasizes testing the fetus. The other options are different contexts: preimplantation genetic testing is done on embryos before implantation in IVF, and anomaly screening focuses broadly on detecting birth defects, often via ultrasound.

Foetal screening is the process of checking the fetus during pregnancy for potential genetic disorders. It aims to estimate the risk of a condition so parents can decide on further testing or management. Noninvasive methods, like analyzing fetal DNA in the mother's blood or using ultrasound markers, are common first steps. If a higher risk is detected, invasive tests such as amniocentesis can provide a definitive diagnosis. Prenatal screening is a closely related term, since prenatal means before birth, but foetal screening specifically emphasizes testing the fetus. The other options are different contexts: preimplantation genetic testing is done on embryos before implantation in IVF, and anomaly screening focuses broadly on detecting birth defects, often via ultrasound.

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