Cargando…
HLA-DRB1*14:54 Is Associated with Pulmonary Alveolar Proteinosis: A Retrospective Real-World Audit
Background: Pulmonary alveolar proteinosis (PAP) is a rare pulmonary disease characterized by abnormal accumulation of pulmonary surfactant lipids in alveoli or terminal bronchioles, leading to increased infection risk and progressive respiratory failure. Approximately more than 90% of all cases are...
Autores principales: | Li, Mengqian, Liu, Qinglin, Wang, Weiwen, Jiang, Lili |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10669482/ https://www.ncbi.nlm.nih.gov/pubmed/38001910 http://dx.doi.org/10.3390/biomedicines11112909 |
Ejemplares similares
-
Pulmonary alveolar proteinosis: An autoimmune disease lacking an HLA association
por: Anderson, Kirsten, et al.
Publicado: (2019) -
Congenital Pulmonary Alveolar Proteinosis
por: Hammami, Saber, et al.
Publicado: (2013) -
Pulmonary alveolar proteinosis in children
por: Bush, Andrew, et al.
Publicado: (2020) -
Familial pulmonary alveolar proteinosis caused by mutations in CSF2RA
por: Suzuki, Takuji, et al.
Publicado: (2008) -
Pulmonary alveolar proteinosis in a cat
por: Szatmári, Viktor, et al.
Publicado: (2015)