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Cystic Fibrosis: A Comprehensive Overview

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1.  What is Cystic Fibrosis?
  1. Progressive, Autosomal recessive genetic disorder
  2. Caused by mutations in the Cystic Fibrosis transmembrane conductance regulator (CFTR) gene
  3. Found on Chromosome 7
  4. All of the above
2.  What is the Gold Standard for diagnosing Cystic Fibrosis?
  1. SWEAT TEST
  2. ABG
  3. EKG
  4. CABG
3.  The multidisciplinary model for Cystic Fibrosis management, REQUIRES the following team members:
  1. Respiratory therapist
  2. Physical therapist
  3. Pharmacist
  4. Research coordinator
4.  The effects of Cystic Fibrosis in the body involve:
  1. Normal breathing
  2. Frequent lung infections
  3. Normal bowel movements
  4. Normal digestion
5.  Identify the following respiratory management and treatments of Cystic Fibrosis:
  1. Pulmonary Function Testing
  2. Bronchodilators
  3. Mucolytics
  4. All of the above

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