Transcript
Page 1: Is It Cystic Fibrosis? Identifying Patients With Atypical CF

Is It Cystic Fibrosis?Identifying Patients With Atypical CF

Page 2: Is It Cystic Fibrosis? Identifying Patients With Atypical CF

The Changing Epidemiology of CF

Page 3: Is It Cystic Fibrosis? Identifying Patients With Atypical CF

The Changing Epidemiology of CF (cont)

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Organ System Involvement in “Classic” CF

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Criteria for CF Diagnosis

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Sweat Chloride Test Results in Patients With CF

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European CF Diagnostic Criteria

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Pancreatic Sufficiency and Residual Function Mutations

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The Continuum of Pancreatic Sufficiency and Genetic Mutations

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Clinical Presentation

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Adult Diagnosis of CF Is Associated With Milder Lung Disease

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Incidence of CFTR Mutations in Patients With Idiopathic

Pancreatitis

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CBAVD

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Clinical Implications of Carrying a 5T Mutation Trans to a Classic CF Mutation

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Clinical Implications of the R117H Mutationa-d

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CFTR Spectruma-e

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CF Diagnostic Categoriesa,b

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CFTR2 Classification of Mutationsa

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When to Suspect CF

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When to Suspect CF (cont)

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Location of Bronchiectasis Can Provide a Clue to the Diagnosis

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What to Do if You Suspect CF

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Abbreviations

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References

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References (cont)

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References (cont)