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Pulmonary Arterial Hypertension (PAH) develops due to the narrowing of the small arteries in the lungs, leading to increased resistance to blood flow. This increased resistance causes the right side of the heart to work harder to pump blood through the lungs, eventually leading to the thickening and stiffening of the pulmonary arteries. The exact cause of PAH can vary and may include genetic factors, underlying medical conditions, or exposure to certain toxins or drugs. Early detection and management of PAH are crucial to prevent further complications and improve quality of life for affected individuals.

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ProfBot

7mo ago

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