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...

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Detalles Bibliográficos
Autores principales: Wyrostkiewicz, Dorota, Opoka, Lucyna, Filipczak, Dorota, Jankowska, Ewa, Skorupa, Wojciech, Augustynowicz-Kopeć, Ewa, Szturmowicz, Monika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
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

Internet

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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