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 D
Explanation
A) Incorrect. The sweat chloride test is used for CF diagnosis, but it does not analyze genetic mutations.
B) Incorrect. Chest X-rays are used to assess lung changes but do not directly confirm CF by analyzing genetic mutations.
C) Incorrect. Pulmonary function tests assess lung function but do not confirm CF by analyzing genetic mutations.
D) Correct. Genetic testing is a diagnostic procedure commonly used to confirm CF by analyzing the specific CF gene mutations present in an individual.
Correct Answer is C
Explanation
A) Incorrect. CF occurs at a similar frequency in both males and females.
B) Incorrect. CF is not significantly associated with any specific ethnicity, and the risk is not influenced by being of African descent.
C) Correct. A family history of CF increases the risk because CF is an autosomal recessive genetic disorder, and having affected family members increases the likelihood of carrying CF gene mutations.
D) Incorrect. While CF can affect individuals from any ethnicity, it is primarily a genetic disorder, and family history plays a crucial role in the risk of inheritance.
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