Recurrence of pulmonary alveolar proteinosis after bilateral lung transplantation in a patient with a nonsense mutation in CSF2RB

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 describe the clin...

詳細記述

保存先:
書誌詳細
出版年:Respir Med Case Rep
主要な著者: Takaki, Masahiro, Tanaka, Takeshi, Komohara, Yoshihiro, Tsuchihashi, Yoshiko, Mori, Daisuke, Hayashi, Kentaro, Fukuoka, Junya, Yamasaki, Naoya, Nagayasu, Takeshi, Ariyoshi, Koya, Morimoto, Konosuke, Nakata, Koh
フォーマット: Artigo
言語:Inglês
出版事項: Elsevier 2016
主題:
Case Report
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4995526/
https://ncbi.nlm.nih.gov/pubmed/27595063
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.rmcr.2016.06.011
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