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Inner cystic fibrosis typically refers to the condition's impact on the internal organs, particularly the lungs and digestive system. Cystic fibrosis is a genetic disorder caused by mutations in the CFTR gene, leading to thick, sticky mucus buildup that obstructs airways and impairs digestion. This can result in chronic respiratory infections, difficulty breathing, and issues with nutrient absorption. Management often involves a combination of medications, physical therapy, and nutritional support to improve quality of life.

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AnswerBot

1d ago

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