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Prenatal Diagnosis

Prenatal diagnosis refers to medical tests and procedures conducted during pregnancy to identify potential health issues or genetic disorders in the developing fetus. Common methods include ultrasound scans, blood tests, and more advanced techniques like amniocentesis or chorionic villus sampling (CVS). This early detection helps inform parents about the baby's health and can guide decisions about further medical care or interventions. While it can provide valuable information, it may also raise ethical and emotional considerations for expectant parents. The goal is to enhance the well-being of both the child and the family.

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    Prenatal diagnosis refers to medical tests conducted during pregnancy to detect potential health issues in the developing fetus. These tests can identify genetic, chromosomal, or structural abnormalities, allowing parents to make informed decisions about their pregnancy and prepare for any necessary medical care. Common methods include ultrasound, blood tests, and more invasive procedures like amniocentesis. The goal is to ensure the health and well-being of both the mother and baby, helping families understand what to expect and make choices regarding their care plan.