Idiopathic pulmonary fibrosis (IPF), formerly known as cryptogenic fibrosing alveolitis, is a rare, chronic, progressive interstitial lung disease.
IPF belongs to the subgroup, known as idiopathic interstitial pneumonia (IIP). It is the most common form of the seven distinct IIPs. Idiopathic means that the cause of the disease by definition is unknown.
IPF is defined as a distinctive type of chronic fibrosing interstitial pneumonia. It is associa...
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Idiopathic pulmonary fibrosis
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