Investigation of Phagocyte Functions in Pseudomonas-Colonized Cystic Fibrosis Patients

Aim: Cystic fibrosis (CF) is an autosomal recessive disorder. Although it is considered as an epithelial disease due to impaired chloride transport, its pathogenesis remains unclear. CF is classified as a syndrome with congenital defects of phagocyte in recent human inborn errors of immunity phenoty...

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Main Authors: Handan Duman Şenol, Meral Barlık, Ezgi Topyıldız, Figen Gülen, Güzide Aksu, Necil Kütükçüler, Esen Demir, Neslihan Edeer Karaca
Format: Article
Language:English
Published: Galenos Publishing House 2024-06-01
Series:Journal of Pediatric Research
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Online Access:https://jpedres.org/articles/investigation-of-phagocyte-functions-in-pseudomonas-colonized-cystic-fibrosis-patients/doi/jpr.galenos.2024.09735
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