Pulmonary Arterial Hypertension (PAH) is a type of pulmonary hypertension caused by thickening and narrowing of the tiny arteries in your lung. This narrowing restricts blood flow through the lungs, raising blood pressure in the lungs. This forces your heart to work harder, and the heart gradually loses its ability to effectively pump blood throughout the body. Pulmonary arterial hypertension (PAH) is a rare, progressive (meaning it worsens over time) disorder with an unknown cause. PAH is most common in women aged 30-60 years. Although there is no cure for PAH, treatments to control symptoms and improve quality of life are available. Among the five types of pulmonary hypertension, PAH is classified as Group 1: PAH. PAH is a rare disease, with only 500-1000 new cases diagnosed in the United States each year. PAH is inherited by approximately 15-20% of patients. Explore more- https://coherentmarketinsightsus.blogspot.com/2022/08/symptoms-of-pulmonary-arterial.html
0 Comments
Leave a Reply. |
Categories
All
|