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Bronchiectasis is characterized by abnormal bronchi dilation and chronic airway infections leading to lung damage, with causes being congenital or acquired. Cystic fibrosis, an autosomal recessive disorder affecting the CFTR gene, results in respiratory and gastrointestinal complications, often diagnosed in childhood. Management of both conditions involves airway clearance, antibiotics, and in some cases, surgical intervention, with a focus on prevention and early treatment of infections.

Author

amnazydan

Language

EN