A nurse is explaining the diagnostic process for cystic fibrosis (CF) to a client and their family. What initial diagnostic test is often used to assess CF in infants who exhibit symptoms suggestive of the condition?
Genetic testing
Sweat chloride test
Chest X-ray
Pulmonary function test
The Correct Answer is B
A) Incorrect. Genetic testing can confirm CF but is not typically the initial diagnostic test used in infants with symptoms suggestive of CF.
B) Correct. The sweat chloride test is often used as the initial diagnostic test to assess for CF in infants who exhibit symptoms.
C) Incorrect. Chest X-rays may be used to assess lung changes in individuals with CF but are not typically the initial diagnostic test in infants.
D) Incorrect. Pulmonary function tests are used to evaluate lung function but are not typically the initial diagnostic test for CF in infants.
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Related Questions
Correct Answer is B
Explanation
A) Incorrect. CF primarily affects the lower respiratory tract, particularly the bronchi and bronchioles, rather than the upper respiratory tract.
B) Correct. CF leads to thickened mucus in the airways, which can cause inflammation, recurrent infections, and progressive lung damage.
C) Incorrect. Enlarged tonsils and adenoids are not a typical manifestation of CF-related respiratory complications.
D) Incorrect. CF affects both the bronchial tubes and the entire respiratory system, often leading to chronic lung infections.
Correct Answer is C
Explanation
A) Incorrect. CF is an autosomal recessive genetic disorder, meaning that both copies of the CFTR gene must carry a mutation for the condition to manifest.
B) Incorrect. CF is not caused by dominant genetic mutations.
C) Correct. CF results from inheriting two recessive genetic mutations, one from each parent, leading to defective CFTR protein function.
D) Incorrect. CF is primarily a genetic disorder with well-established genetic mutations associated with its development.
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