Various procedures can be used to detect genetic disorders before birth. Among the tests discussed in this chapter, which is the least invasive (list first), and which two allow the chromosomes of the fetus to be examined? See Concept 14.4 (Page)

Question

Biology

Jada Kline

7 October, 19:42

Various procedures can be used to detect genetic disorders before birth. Among the tests discussed in this chapter, which is the least invasive (list first), and which two allow the chromosomes of the fetus to be examined? See Concept 14.4 (Page)

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Answers (1)

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Reuben Ellis · Answer 1

Ultrasound Imaging

Chorionic Villus Sampling and Amniocentesis

Explanation:

Ultrasound Imaging is used to detect the genetic disorders or syndrome of the foetus. It involves the use high frequency sound waves. The ultrasounds of first, second and third trimester provides the information about any abnormalities of the foetus.

Chorionic villus sampling (CVS) and Amniocentesis is the method that allows the examination of chromosomes of the foetus. In CVS, small amount of placenta is taken as a sample whereas in amniocentesis, small amount of amniotic fluid is taken and examined.