Idiopathic Pulmonary Fibrosis

Idiopathic pulmonary fibrosis (IPF) is a chronic lung disease characterized by progressive scarring (fibrosis) of the lung tissue without a known cause. This scarring makes it difficult for the lungs to function properly, leading to shortness of breath and decreased oxygen levels in the blood. Treatment may include medications, oxygen therapy, and, in severe cases, lung transplantation.

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