Pulmonary arterial hypertension (PAH) is a rare, progressive respiratory disease characterised by dangerously high blood pressure and vascular resistance; this causes progressive fatigue in the right ventricle that can culminate in even fatal heart failure.
Symptoms are breathlessness, dizziness and fatigue.
Pulmonary arterial hypertension is classified as a sub-category of pulmonary hypertension: in Italy, it is estimated there are about 2,000 patients with severe PAH.
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