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Elderly-onset hereditary pulmonary alveolar proteinosis and its cytokine profile
BACKGROUND: Pulmonary alveolar proteinosis (PAP) is a rare lung disease characterized by surfactant accumulation, and is caused by disruption of granulocyte/macrophage colony-stimulating factor (GM-CSF) signaling. Abnormalities in CSF2 receptor alpha (CSF2RA) were reported to cause pediatric heredit...
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| Veröffentlicht in: | BMC Pulm Med |
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| Hauptverfasser: | , , , , , , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BioMed Central
2017
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5316164/ https://ncbi.nlm.nih.gov/pubmed/28212655 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12890-017-0382-x |
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