A client is inquiring about the genetic basis of cystic fibrosis (CF). Which statement by the nurse provides an accurate explanation?
"CF is caused by a dominant genetic mutation that always manifests in affected individuals."
"CF results from the presence of two recessive genetic mutations, one inherited from each parent."
"CF is due to a spontaneous genetic mutation that occurs during a person's lifetime."
"CF is exclusively caused by environmental factors and is not related to genetics."
The Correct Answer is B
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) Correct. CF is caused by the inheritance of two recessive genetic mutations, one from each parent, resulting in defective CFTR protein function.
C) Incorrect. CF is primarily a genetic disorder present from birth, not one caused by spontaneous mutations during a person's lifetime.
D) Incorrect. CF is primarily a genetic disorder with well-established genetic mutations associated with its development.
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is C
Explanation
A) Incorrect. PERT is not primarily used to control blood sugar levels; it is used to improve nutrient absorption.
B) Incorrect. While CF management aims to improve lung function, PERT is specifically used to address pancreatic insufficiency and digestive issues.
C) Correct. The primary purpose of PERT in CF management is to replace the missing digestive enzymes and aid in the digestion of fats and nutrients.
D) Incorrect. PERT does not increase mucus production in the airways; it is focused on the digestive system.
Correct Answer is B
Explanation
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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