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Pathophysiology Exam 1 Comprehensive Resource To Help You Ace Exams Includes Frequently Tested Questions With ELABORATED 100% Correct COMPLETE SOLUTIONS Guaranteed Pass First Attempt!! Current Update!! Instant Download Pdf!!

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Pathophysiology Exam 1 Comprehensive Resource To Help You Ace Exams Includes Frequently Tested Questions With ELABORATED 100% Correct COMPLETE SOLUTIONS Guaranteed Pass First Attempt!! Current Update!! Instant Download Pdf!! 1. 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 Answer: c 2. An error in which homologous chromosomes fail to separate during meiosis is termed: A) aneuploidy. B) nondisjunction. C) polyploidy. D) anaplasia. - Correct Answer: b 3. 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 Answer: a 4. 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 Answer: c 5. 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 Answer: b 6. The most common cause of Down syndrome is: A) paternal nondisjunction. B) maternal translocations. C) maternal nondisjunction. D) paternal translocations. - Correct Answer: c 7. 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 Answer: d 8. 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 Answer: c 9. 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 Answer: c 10. 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 Answer: d

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Pathophysiology Exam 1

Comprehensive Resource To Help You Ace 2026-2027
Exams Includes Frequently Tested Questions With
ELABORATED 100% Correct COMPLETE SOLUTIONS

Guaranteed Pass First Attempt!! Current Update!!

Instant Download Pdf!!




1. 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 Answer: c


2. An error in which homologous chromosomes fail to separate during meiosis
is termed:
A) aneuploidy.
B) nondisjunction.
C) polyploidy.
D) anaplasia. - Correct Answer: b


3. 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 Answer: a

,4. 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 Answer: c


5. 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 Answer: b


6. The most common cause of Down syndrome is:
A) paternal nondisjunction.
B) maternal translocations.
C) maternal nondisjunction.
D) paternal translocations. - Correct Answer: c


7. 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 Answer: d

,8. 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 Answer: c


9. 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 Answer: c


10.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 Answer: d


11.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 Answer: d

, 12.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 Answer: b


13.Cystic fibrosis is caused by an _____ gene.
A) X-linked dominant
B) X-linked recessive
C) autosomal dominant
D) autosomal recessive - Correct Answer: d


14.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 Answer: b


15.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 Answer: b


16.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

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