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Cystic Fibrosis: Management

Cystic Fibrosis: Management

Cystic fibrosis (CF) is an autosomal recessive disorder that predominantly affects individuals of Northern European descent, occurring at a rate of 1 in 3500. It is caused by a genetic mutation in a gene on chromosome 7, most commonly the ΔF508 mutation, that codes for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. This results in thicker mucus secretions and obstruction pathologies in multiple organs, including the lungs and sinuses.
Sinus disease and chronic...

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Machine learning evaluates improvement in sinus computed tomography opacification with CFTR modulator therapy

Daniel M Beswick¹, Stephen M Humphries², Connor D Balkissoon³

¹Department of Otolaryngology-Head and Neck Surgery, University of California, Los Angeles, CA.

International Forum of Allergy & Rhinology

|November 3, 2020

Summary

No abstract available in PubMed .

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