Using both non-invasive and invasive procedures, the fetus is examined for any genetic or chromosomal abnormalities. Conditions like cystic fibrosis and Down Syndrome can be identified at an initial stage and treated accordingly.
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A painless procedure involving the insertion of a probe or needle inside the uterus for detailed fetal examination.
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Non-Invasive Prenatal Screening analyses DNA samples of the baby to evaluate possible chromosomal conditions during the pregnancy.
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