Diagnosing cystic fibrosis in low- and middle-income countries: challenges and strategies

Abstract Background Cystic Fibrosis is caused by recessively inherited variants of the cystic fibrosis transmembrane regulator. It is associated with diverse clinical presentations that can affect the respiratory, digestive, and reproductive systems and inhibit nutrient absorption and growth. Main B...

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Bibliographic Details
Main Authors: Michèle Fuhrer, Marco Zampoli, Hugues Abriel
Format: Article
Language:English
Published: BMC 2024-12-01
Series:Orphanet Journal of Rare Diseases
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Online Access:https://doi.org/10.1186/s13023-024-03506-1
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