Stem Cell Treatment for Pulmonary Arterial Hypertension
08/01/2024
In the first case of its kind, a young girl suffering from PAH has shown significant improvement after receiving an experimental stem cell treatment.
Read on to find out more about this story.
What is Pulmonary Arterial Hypertension?
PAH (Pulmonary Arterial Hypertension) is a condition that affects the blood vessels that supply the lungs causing high blood pressure. The walls of the arteritis become stiff making it difficult for them to expand correctly to allow proper blood flow. The reduced blood flow causes the right side of the heart to work harder, slowly becoming weaker which can lead to heart failure.
Symptoms of Pulmonary Hypertension include:
-
Feeling faint and dizzy
-
Shortness of breath
-
Chest pains
-
Racing heartbeat
-
Shortness of breath
-
Swelling