A birth defect is an issue in the development or operation of a baby's body parts. The issue is present from birth, albeit it might not be identified for some time. There are instances where the issue is inherited (passed down in families). The cause is frequently unknown. Certain congenital abnormalities, often known as birth defects, are modest and don't require medical attention. Some may be more serious and need ongoing care. Typically, genetic testing on little blood or saliva samples is used to identify birth abnormalities. Tests can be performed prior to delivery, immediately postpartum (for example, newborn screening), or at a later time. Genetic testing can also be performed on the placenta (by chorionic villus sample) or amniotic fluid (via amniocentesis) during pregnancy. In vitro fertilization may also involve genetic testing. Before the embryo is implanted into the uterus, it can be tested.
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