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    Idiopathic Pulmonary Fibrosis

    Idiopathic Pulmonary Fibrosis: is a type of lung disease that results in scarring (fibrosis) of the lungs for an unknown reason. Over time, the scarring gets worse and it becomes hard to take in a deep breath, as a result the lungs cannot take in enough oxygen. Lung tissue becomes scarred and changes the lung's ability to function normally. The scarring typically starts on the outside edges of the lungs and eventually advances towards the center of the lungs. IPF is a disabling disease without a known cure.

    Trending News

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      Researchers behind a large trial of antibiotics for chronic lung diseases have found that that the drugs are ineffective ...
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      JUL 23, 2020
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      In the past year, biomedical engineers have created lab-grown heart cells, retinal nerve cells, and even vocal cords tha ...
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      Limber Lungs: One Type of Airway Cell Can Regenerate Another Lung Cell Type
      APR 16, 2015
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      A new collaborative study describes a way that lung tissue can regenerate after injury. The team found that lung tissue ...
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      DEC 08, 2013
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    DEC 08, 2013
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