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Pulmonary alveolar proteinosis: diagnostic and therapeutic challenges
Pulmonary Alveolar Proteinosis (PAP) is a rare syndrome characterized by pulmonary surfactant accumulation within the alveolar spaces. It occurs with a reported prevalence of 0.1 per 100,000 individuals and in distinct clinical forms: autoimmune (previously referred to as the idiopathic form, repres...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BioMed Central
2012
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3415123/ https://ncbi.nlm.nih.gov/pubmed/22958344 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2049-6958-7-4 |
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