HyperTension FAQ
Who Group 1 Pulmonary Arterial Hypertension
Pulmonary Arterial Hypertension (PAH) is a rare, yet progressively debilitating condition characterized by high blood pressure in the arteries of the lungs. Group 1 PAH, specifically, refers to a subcategory of this disease distinguished by its own unique pathophysiology and causes. Conditions in this group are often idiopathic, heritable, or associated with other conditions such as connective tissue disorders, congenital heart disease, or drug use. What makes Group 1 PAH particularly challenging is its complexity, and while there’s no cure, effective management can significantly improve quality of life.
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