- Abnormal chloride channel function, leading to thick, viscous secretions.
- Impaired ciliary movement.
- Alveolar destruction.
- Bronchial hypersensitivity.
26. A 25-year-old male with a history of recurrent infections, particularly pneumonia, presents with chronic productive cough, bronchiectasis on CT scan, and steatorrhea. What is the technical primary pathophysiological defect in cystic fibrosis?
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