Amniocentesis is a procedure used to diagnose
fetal defects in the early second trimester of pregnancy. A sample of the amniotic
fluid, which surrounds a fetus in the womb, is collected through a pregnant
woman’s abdomen using a needle and syringe. Tests performed on fetal cells
found in the sample can reveal the presence of many types of genetic
disorders, thus allowing doctors and prospective parents to make important decisions about early treatment and intervention.
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