Idiopathic pulmonary fibrosis (IPF) is a disease that causes scarring in the lungs and serious shortness of breath.
A research group at the Lulu Owen School of Medicine based at Vanderbilt University Medical Center (VUMC), has received an $11 million grant from the National Heart, Lung and Blood Institute to continue studying specific genes that have been found in family members with idiopathic pulmonary fibrosis.
In partnership with the University of Chicago, the research group is using genetic material from more than 1,200 families with IPF and hopes to continue its investigation into genetic mutations and how genes affect both sporadic (once in a family) and familial idiopathic pulmonary fibrosis (more than once case in a family).
Between 10% and 20% of people with IPF have at least one family member who also has the disease.
Pulmonary Fibrosis News is strictly a news and information website about the disease. It does not provide medical advice, diagnosis or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or another qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website.
We are sorry that this post was not useful for you!
Let us improve this post!
Tell us how we can improve this post?