Recurrence of pulmonary alveolar proteinosis after bilateral lung transplantation in a patient with a nonsense mutation in CSF2RB
Abstract Hereditary pulmonary alveolar proteinosis (PAP) caused by mutations in CSF2RA or CSF2RB , which encode GM-CSF receptor α and β respectively, is a rare disease. Although some experimental therapeutic strategies have been proposed, no clinical evidence has yet been reported. We herein describ...
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Veröffentlicht in: | Respiratory medicine case reports 2016-01, Vol.19, p.89-93 |
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Hauptverfasser: | , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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