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Examen

Pathophysiology Exam

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The Pathophysiology Exam evaluates a student's understanding of the physiological processes underlying disease. It covers the mechanisms of cellular injury, inflammation, immune responses, genetic and environmental influences on health, and alterations in major body systems such as cardiovascular, respiratory, renal, neurological, and endocrine systems. Students are expected to apply critical thinking to explain how normal body functions are disrupted by disease and how these changes manifest clinically. This knowledge is essential for accurate assessment, diagnosis, and the development of appropriate nursing interventions.

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PATHOPHYSIOLOGY EXAM
Actual Questions and Answers
Expert-Verified Explanation
This Exam contains:
✪ 50 Questions and Answers
✪ Multiple-choice and True/False Format
✪ Expert-Verified Explanations
✪ Verified with Trusted Textbooks



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
Answer: C
EXPLANATION: A karyotype is a photograph of chromosomes arranged by size, shape, and
number for analysis.



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

A) aneuploidy
B) nondisjunction
C) polyploidy
D) anaplasia
Answer: B
EXPLANATION: Nondisjunction results in gametes with abnormal numbers of chromosomes,
leading to chromosomal disorders.



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
Answer: A

, EXPLANATION: Aneuploid cells have a chromosome number that is not an exact multiple of
23, leading to genetic abnormalities.



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
Answer: C
EXPLANATION: Tetraploidy means the fetus has four complete sets of chromosomes (92
total), which is incompatible with life.



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
Answer: B
EXPLANATION: A mosaic has two or more cell lines with different karyotypes, potentially
resulting in milder disease expression.



6. The most common cause of Down syndrome is:

A) paternal nondisjunction
B) maternal translocations
C) maternal nondisjunction
D) paternal translocations
Answer: C
EXPLANATION: Maternal nondisjunction during meiosis is responsible for most cases of
trisomy 21 (Down syndrome).



7. Risk factors for Down syndrome include:

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Subido en
1 de julio de 2025
Número de páginas
14
Escrito en
2024/2025
Tipo
Examen
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