Idiopathic Pulmonary Fibrosis

Idiopathic Pulmonary Fibrosis

Idiopathic Pulmonary Fibrosis is a chronic, progressive lung disease characterised by scarring of lung tissue, leading to severe breathing difficulties. The exact cause of Idiopathic Pulmonary Fibrosis remains unknown, and it primarily affects individuals over 50. Treatment options focus on slowing disease progression and managing symptoms. Diagnosis typically involves high-resolution CT scans and lung biopsies.