Idiopathic Pulmonary Fibrosis (IPF)
Idiopathic Pulmonary Fibrosis (IPF) is a chronic, progressive lung disease characterized by scarring (fibrosis) of lung tissue. This scarring leads to a decline in lung function, making it increasingly difficult to breathe. IPF typically affects older adults and has no known cure, though treatments can manage symptoms and slow disease progression. Causes and Risk Factors