A nurse is educating a client about the diagnostic evaluation of cystic fibrosis (CF). What test is commonly used to screen for CF in newborns shortly after birth?
Sweat chloride test
Chest X-ray
Pulmonary function test
Complete blood count (CBC)
The Correct Answer is A
A) Correct. The sweat chloride test is commonly used for newborn screening for CF. Elevated sweat chloride levels are indicative of CF.
B) Incorrect. Chest X-rays may be used to assess lung changes in individuals with CF but are not a primary diagnostic test, especially in newborns.
C) Incorrect. Pulmonary function tests are used to evaluate lung function but are not typically performed as part of newborn screening for CF.
D) Incorrect. A complete blood count (CBC) is a general blood test and is not specific for CF diagnosis.
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Related Questions
Correct Answer is D
Explanation
A) Incorrect. If both parents are carriers, their child's risk of having CF is 25%, not 50%.
B) Incorrect. While the risk is increased, having two carrier parents does not guarantee that a child will have CF.
C) Incorrect. If both parents are carriers, their child can inherit two normal genes (no CF), one normal and one CF gene (carrier status), or two CF genes (CF).
D) Correct. When both parents are carriers, there is a 25% chance that their child will inherit two CF genes and have CF, a 50% chance of being a carrier, and a 25% chance of inheriting two normal genes (no CF).
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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