Prenatal diagnosis

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Prenatal Diagnosis is a medical procedure used to detect abnormalities in a developing fetus during pregnancy. This procedure can include a variety of tests and screenings that can provide information about the baby's health before it is born.

Overview[edit | edit source]

Prenatal diagnosis is a part of prenatal care that involves testing for diseases or conditions in a fetus or embryo before it is born. The tests can detect a variety of conditions, such as genetic disorders, congenital abnormalities, and chromosomal abnormalities. The results can help doctors and parents make informed decisions about the pregnancy and prepare for any special care the baby might need.

Types of Prenatal Diagnosis[edit | edit source]

There are several types of prenatal diagnosis, including:

  • Ultrasound: This is a non-invasive procedure that uses sound waves to create images of the fetus in the womb. It can detect physical abnormalities and monitor the baby's growth and development.
  • Amniocentesis: This is a diagnostic test that involves removing a small amount of amniotic fluid from the womb to test for genetic disorders and chromosomal abnormalities.

Risks and Benefits[edit | edit source]

Like any medical procedure, prenatal diagnosis has potential risks and benefits. The benefits include early detection of potential health problems, which can allow for early intervention or treatment. The risks can include physical risks to the mother or baby, as well as the potential for false-positive or false-negative results.

Ethical Considerations[edit | edit source]

Prenatal diagnosis also raises ethical issues, such as the potential for discrimination or stigmatization of individuals with genetic disorders, and the potential for selective abortion based on the results of prenatal testing.

See Also[edit | edit source]

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Contributors: Prab R. Tumpati, MD