Unique marker for pericytes could help forge new path for pulmonary hypertension care

Pulmonary arterial hypertension (PAH) is a rare condition that’s difficult to treat. The hallmarks of the disease—narrowing of the arterioles and capillaries that deliver blood to the lungs—force the heart to work harder. In severe cases, PAH can lead to heart failure.

This article was originally published on MedicalXpress.com

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