Congenital Anomalies Diagnosis

Congenital anomalies are health conditions or physical differences present at birth, resulting from abnormal development during pregnancy. They can affect various parts of the body, including organs, limbs, and facial features, and can be caused by genetic factors, environmental influences, or a combination of both. Diagnosis typically involves prenatal screenings, imaging tests like ultrasounds, and examinations after birth. Early identification can help healthcare providers plan appropriate treatments or interventions, improving outcomes for affected individuals. Understanding these anomalies is important for better health support and management throughout life.