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Pathophysiology of Disease An Introduction to Clinical Medicine 8th Edition Actual Exam Questions & 100% Correct Answers | Hammer McPhee

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Pathophysiology of Disease An Introduction to Clinical Medicine 8th Edition Actual Exam Questions & 100% Correct Answers | Hammer McPhee | latest update 2025/2026 already graded A+

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Pathophysiology of Disease An Introduction to Clinical Medicine 8th Edition
Actual Exam Questions & 100% Correct Answers | Hammer McPhee

Multiple Choices

QUESTION: An ordered photographic display of a set of chromosomes from a single cell is a(n):

A) metaphase spread.

B) autosomal spread.

C) karyotype.

D) anaphase spread. - Correct Ans- c




QUESTION: An error in which homologous chromosomes fail to separate during meiosis is termed:

A) aneuploidy.

B) nondisjunction.

C) polyploidy.

D) anaplasia. - Correct Ans- b




QUESTION: A somatic cell that does not contain a multiple of 23 chromosomes is called:

A) an aneuploid cell.

B) a euploid cell.

C) a polyploidy cell.

D) a haploid cell. - Correct Ans- a




QUESTION: A 20-year-old pregnant female gives birth to a stillborn child. Autopsy reveals that the fetus has 92
chromosomes. Which of the following describes this condition?

A) Euploidy

B) Triploidy

C) Tetraploidy

D) Aneuploidy - Correct Ans- c


1|Page

,QUESTION: If a person is a chromosomal mosaic, the person may:

A) be a carrier of the genetic disease.

B) have a mild form of the genetic disease.

C) have two genetic diseases.

D) be sterile as a result of the genetic disease. - Correct Ans- b




QUESTION: The most common cause of Down syndrome is:

A) paternal nondisjunction.

B) maternal translocations.

C) maternal nondisjunction.

D) paternal translocations. - Correct Ans- c




QUESTION: Risk factors for Down syndrome include:

A) fetal exposure to mutagens in the uterus.

B) increased paternal age.

C) family history of Down syndrome.

D) pregnancy in women over age 35. - Correct Ans- d




QUESTION: A 13-year-old girl has a karyotype that reveals an absent homologous X chromosome with only a
single X chromosome present. Her condition is called:

A) Down syndrome.

B) Cri du chat syndrome.

C) Turner syndrome.

D) Edward syndrome - Correct Ans- c




2|Page

,QUESTION: A child is diagnosed with cystic fibrosis. History reveals that the child's parents are first cousins.
Cystic fibrosis was most likely the result of:

A) X inactivation.

B) genomic imprinting.

C) consanguinity.

D) obligate carriers. - Correct Ans- c




QUESTION: Joey, age 9, is admitted to a pediatric unit with Duchenne muscular dystrophy. He inherited this
condition through a:

A) sex-linked dominant trait.

B) sex-influenced trait.

C) sex-limited trait.

D) sex-linked recessive trait. - Correct Ans- d




QUESTION: A 50-year-old male was recently diagnosed with Huntington disease. Transmission of this disease is
associated with:

A) penetrance.

B) recurrence risk.

C) expressivity.

D) delayed age of onset. - Correct Ans- d

QUESTION: People who have neurofibromatosis will show varying degrees of the disease; this is because of
the genetic principle of:

A) penetrance.

B) expressivity.

C) dominance.

D) recessiveness. - Correct Ans- b




QUESTION: Cystic fibrosis is caused by an _____ gene.

3|Page

, A) X-linked dominant

B) X-linked recessive

C) autosomal dominant

D) autosomal recessive - Correct Ans- d




QUESTION: To express a polygenic trait:

A) genes must interact with the environment.

B) several genes must act together.

C) multiple mutations must occur in the same family.

D) in situ cloning must occur. - Correct Ans- b




QUESTION: The gradual increase in height among the human population over the past 100 years is an example
of:

A) polygenic trait.

B) multifactorial trait.

C) crossing over.

D) recombination. - Correct Ans- b




QUESTION: A couple has three offspring: one child with an autosomal dominant disease trait and two who are
normal. The father is affected by the autosomal dominant disease, but the mother does not have the disease
gene. What is the recurrence risk of this autosomal dominant disease for their next child?

A) 50%

B) 33%

C) 25%

D) Impossible to determine - Correct Ans- a




QUESTION: A 12-year-old male is diagnosed with Klinefelter syndrome. His karyotype would reveal which of
the following?

4|Page

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Subido en
7 de julio de 2025
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