Children with cystic fibrosis require comprehensive medical assistance, including regular pulmonary care to manage lung function and prevent infections, which may involve airway clearance techniques and inhaled medications. They also need nutritional support, including pancreatic enzyme replacements and a high-calorie diet to address malabsorption issues. Routine monitoring by a multidisciplinary team, including pulmonologists, dietitians, and physical therapists, is essential for managing the condition effectively and improving quality of life.
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