Chapter 8: Overview of Genetics and Genomics in Nursing - Nurselytic

Questions 40

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Brunner & Suddarth's Textbook of Medical-Surgical Nursing 14e (Hinkle 2017)

Chapter 8 : Overview of Genetics and Genomics in Nursing Questions

Question 1 of 5

What sign should the nurse instruct the woman to look for in the new baby?

Correct Answer: C

Rationale: Physical assessment may provide clues that a particular genetic condition is present. For neurofibromatosis type 1, skin findings like caf-au-lait spots are a key indicator. Increased urination might suggest diabetes, projectile vomiting could indicate pyloric stenosis, and xanthomas are associated with hyperlipidemia, not neurofibromatosis.

Question 2 of 5

What should the nurse do?

Correct Answer: D

Rationale: The nurse must honor the patient's wishes while explaining the potential benefit this information may have for other family members. Breaching confidentiality by contacting siblings or their physicians is unethical. Involving a geneticist may be helpful, but the primary action is to respect the patient's confidentiality while encouraging disclosure.

Question 3 of 5

What is the chance that this couple will have a child with six toes?

Correct Answer: A

Rationale: When two carrier parents have children together, they have a 25% chance of having a child who inherits the gene mutation from each parent and who will have the condition, as in autosomal recessive inheritance. The other percentages are incorrect for this inheritance pattern.

Question 4 of 5

The nurse informs the patient that genetic counseling and prenatal testing should be performed for all pregnant women in which age group?

Correct Answer: C

Rationale: Women who are 35 years of age or older have an increasing chance of giving birth to infants with chromosomal differences, such as trisomy 21. For this reason, genetic counseling and prenatal testing are recommended for all pregnant women above this age.

Question 5 of 5

What is an essential component of care for this patient?

Correct Answer: D

Rationale: The provision of genetic counseling, evaluation, and testing for the disease is essential in care, especially given the family history of Huntington disease. This encompasses assessing risks to offspring and addressing symptoms, making it the most comprehensive option.

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