
Cystic fibrosis (CF) is a complex genetic disorder with significant implications for those affected. While there is currently no cure, advancements in our understanding of the disease, its genetic underpinnings, and the development of targeted therapies like CFTR modulators are improving both life expectancy and quality of life for those affected. Ongoing research into gene therapy, modifier genes and personalized medicine holds much promise for the future management of CF.
A few sources: https://www.nhs.uk/conditions/cystic-fibrosis/; https://my.clevelandclinic.org/health/diseases/9358-cystic-fibrosis; https://www.nhlbi.nih.gov/health/cystic-fibrosis/living-with; https://pmc.ncbi.nlm.nih.gov/articles/PMC4364438/
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