Question

Question 9 of 10 > Match each statement to the genetic screening procedure it describes. Newborn screening Heterozygote screening Prenatal diagnosis Presymptomatic testing Answer Bank identifies treatable genetic disorders soon after birth identifies recessive disease carriers in a population identifies genetic disorders in a developing fetus identifies a genetic disease in a healthy, but high-risk, patient

Answer 1

Explain Newborn Screening > Answer Identified treatable genetic disorders soon after birth. toota This screening test look for genetic disorder in the new-born bady. In addition to blood test, screeing test for hearing loss & Critical congenital disea heart disease (CCHD) is recommended for all new-born Heterozygote screening Answer: Identifies reccessive diseases carrers in a population. This is a screening programme, the conduct of the test is not restricted to a single person instead the entire group is tested, to prevent genetic hereditory disorders

Prenatal screening » Answers Identities genetic disorder in developing fetus Explain Prenatal screening test can identity, whether your baby is more or less likely to have Certain birth defects, many of which are genetic disorder. This test includes blood tests, a specific type of ultrasound att prenotal cell-free DNA screening Answer Presumptomatic screening Identities a genetic disease in a healthy but high risk patient. Explain -> o It is a form of Predictive testing, used to detect gene mutations associated with disorders that appears after birth often later in life.