A novel immunodeficiency syndrome as a rare cause of secondary pulmonary alveolar proteinosis: A diagnosis after 5 decades
Case report of a male patient with a five-decade follow-up history in a tertiary care hospital distinguished for malabsorption syndrome, failure-to-thrive, meningitis and recurrent bacterial, fungal and mycobacterial pulmonary infections. Additionally, he developed epider- modysplasia verruciformis,...
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| Vydáno v: | Revista Portuguesa de Pneumología |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Sociedade Portuguesa de Pneumologia
2014
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| Témata: | |
| On-line přístup: | https://www.redalyc.org/articulo.oa?id=169731783009 |
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