201 top medical experts on Acquired Pulmonary Alveolar Proteinosis across 13 countries and 8 U.S. states, including 42 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Acquired Pulmonary Alveolar Proteinosis: A rare primary interstitial lung disease characterized by the accumulation of lipids and proteins related to surfactant in the alveoli in association with the presence of antibodies against granulocyte-macrophage colony-stimulating factor (GM-CSF). The disease leads to a progressive impairment of gas exchange and respiratory insufficiency.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations

Social Networking Websites

  • A Yahoo Group is available for pulmonary alveolar proteinosis. You can connect with others through this forum. GARD does not monitor their messages, so please use your own discretion when using this group.
  • Synonyms: Acquired Pulmonary Alveolar Lipoproteinosis,  Autoimmune Pulmonary Alveolar Proteinosis


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