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Merck Manual
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Pediatrics
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Cystic Fibrosis (CF)
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Cystic Fibrosis (CF)
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Cystic Fibrosis
General reference
Etiology
Pathophysiology
Respiratory
Gastrointestinal
Other
Symptoms and Signs
Respiratory
Gastrointestinal
Other
Diagnosis
Newborn screening
Sweat testing
Intermediate sweat test results
CFTR-related metabolic syndrome and CF screen positive, inconclusive diagnosis
Pancreatic tests
Respiratory assessment
Carrier screening
Diagnosis reference
Treatment
Treatment of respiratory manifestations
CFTR modulators
Treatment and prevention of infections
Treatment of gastrointestinal manifestations
Treatment of other manifestations
Treatment references
Prognosis
End-of-life care
Prognosis reference
Key Points
More Information