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Nontuberculous Mycobacterial Lung Disease in the Patients with Cystic Fibrosis—A Challenging Diagnostic Problem
Background: Cystic fibrosis (CF) is an autosomal, recessive genetic disorder, caused by a mutation in the cystic fibrosis transmembrane conductance receptor regulator (CFTR) gene. Dysregulated mucous production, and decreased bronchial mucociliary clearance, results in increased susceptibility to ba...
Autores principales: | Wyrostkiewicz, Dorota, Opoka, Lucyna, Filipczak, Dorota, Jankowska, Ewa, Skorupa, Wojciech, Augustynowicz-Kopeć, Ewa, Szturmowicz, Monika |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9316837/ https://www.ncbi.nlm.nih.gov/pubmed/35885420 http://dx.doi.org/10.3390/diagnostics12071514 |
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