Overview of Pulmonary arterial hypertension (PAH)

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Pulmonary arterial hypertension (PAH) is a rare and progressive disorder of the lungs that causes high blood pressure in the arteries of the lungs. It is a serious and potentially life-threatening condition that can lead to severe disability and even death. The condition occurs when the walls of the pulmonary arteries become thickened and stiffened, forcing the heart to work harder to pump blood through them.

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