Long-term follow-up and treatment of congenital alveolar proteinosis

BACKGROUND: Clinical presentation, diagnosis, management and outcome of molecularly defined congenital pulmonary alveolar proteinosis (PAP) due to mutations in the GM-CSF receptor are not well known. CASE PRESENTATION: A 2 1/2 years old girl was diagnosed as having alveolar proteinosis. Whole lung l...

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Detalles Bibliográficos
Autores principales: Griese, Matthias, Ripper, Jan, Sibbersen, Anke, Lohse, Pia, Lohse, Peter, Brasch, Frank, Schams, Andrea, Pamir, Asli, Schaub, Bianca, Muensterer, Oliver J, Schön, Carola, Glöckner-Pagel, Judith, Nicolai, Thomas, Reiter, Karl, Hector, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3175167/
https://www.ncbi.nlm.nih.gov/pubmed/21849033
http://dx.doi.org/10.1186/1471-2431-11-72

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3175167/
https://www.ncbi.nlm.nih.gov/pubmed/21849033
http://dx.doi.org/10.1186/1471-2431-11-72

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