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Congenital anomalies of pulmonary arteries
by Alike Medical Team ∙ Updated on June 13, 2023
Pulmonary atresia is a congenital defect that typically is diagnosed soon after birth. In this condition, the valve through which blood flows from the heart to the lungs, does not form correctly. The blood finds other passages to flow to the lungs, within the heart and its arteries, which are closed soon after birth. This condition is life threatening, and has to be treated for the baby to live. Risk factors for pulmonary atresia is a parent or sibling ith this condition, a mother who was obese before pregancy, smooking before or during preganncy, a mother with uncontrolled diabetes, and maternal usage of severeal medications.
4 people with Congenital anomalies of pulmonary arteries are on Alike.
Symptoms of pulmonary atresia may include a blue or gray tones skin baby, difficulty to breath, feeding problems, and fatigue.
Diagnosis of pulmonary atresia may include pulse oximetry, chest X-ray, ECG, echocardiogram, cardiac catheterization, and a CT-scan.
Treatment for pulmonary atresia are prostaglandins to prevent the closure of the ductus arteriosus, so that blood can continue to flow, just until the correction of the atresia. Procedure for correction of the abnormality are either via catheterization or open heart surgeries.
☝ We provide information on prescription and over-the-counter medicines, diagnosis, procedures and lab tests. This material is provided for educational purposes only and is not medical advice, diagnosis or treatment.
National Institutes of Health ∙ World Health Organization ∙ MedlinePluse ∙ Centers for Disease Control and Prevention
☝ All information has been reviewed by certified physicians from Alike
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