Podcast
Questions and Answers
Why is newborn screening for cystic fibrosis important?
Why is newborn screening for cystic fibrosis important?
- To identify digestive issues
- To detect lung infections
- To diagnose respiratory symptoms
- To allow for early detection and intervention (correct)
What is the primary purpose of genetic testing for cystic fibrosis?
What is the primary purpose of genetic testing for cystic fibrosis?
- To diagnose respiratory symptoms
- To identify specific CFTR gene mutations (correct)
- To detect digestive issues
- To identify lung infections
Why do dentists need to be cautious when treating patients with cystic fibrosis?
Why do dentists need to be cautious when treating patients with cystic fibrosis?
- Because of potential medication interactions
- Because of compromised immune function
- Because of respiratory complications
- All of the above (correct)
What is the difference in life expectancy between male and female patients with cystic fibrosis?
What is the difference in life expectancy between male and female patients with cystic fibrosis?
What can preventive dental care help prevent in individuals with cystic fibrosis?
What can preventive dental care help prevent in individuals with cystic fibrosis?
Why may CF patients have difficulty tolerating certain dental equipment or procedures?
Why may CF patients have difficulty tolerating certain dental equipment or procedures?
What is the primary reason for the high incidence of tooth discoloration in patients with cystic fibrosis?
What is the primary reason for the high incidence of tooth discoloration in patients with cystic fibrosis?
What is a common respiratory symptom in patients with cystic fibrosis?
What is a common respiratory symptom in patients with cystic fibrosis?
Why do patients with cystic fibrosis have a lower caries rate?
Why do patients with cystic fibrosis have a lower caries rate?
What is a common dental issue in patients with cystic fibrosis due to chronic nasal and sinus obstruction?
What is a common dental issue in patients with cystic fibrosis due to chronic nasal and sinus obstruction?
What type of mutation is responsible for approximately 70% of affected alleles in Cystic Fibrosis?
What type of mutation is responsible for approximately 70% of affected alleles in Cystic Fibrosis?
What is the primary function of the CFTR gene in the human body?
What is the primary function of the CFTR gene in the human body?
What is a common symptom of Cystic Fibrosis that affects the digestive system?
What is a common symptom of Cystic Fibrosis that affects the digestive system?
What is the name of the gene responsible for Cystic Fibrosis?
What is the name of the gene responsible for Cystic Fibrosis?
What is the location of the CFTR gene?
What is the location of the CFTR gene?
What is the primary function of the CFTR protein in the body?
What is the primary function of the CFTR protein in the body?
What happens to the mucus covering the cells when the CFTR protein is not working correctly?
What happens to the mucus covering the cells when the CFTR protein is not working correctly?
What is the result of the dysfunctional CFTR protein in the respiratory epithelium?
What is the result of the dysfunctional CFTR protein in the respiratory epithelium?
What is the effect of the impaired CFTR protein on the airway surface layer?
What is the effect of the impaired CFTR protein on the airway surface layer?
What is the geographic distribution of cystic fibrosis?
What is the geographic distribution of cystic fibrosis?
