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Test Bank For Pathophysiology: A Practical Approach 5th Edition by Lachel Story, ISBN NO: 9781284288094| Complete Guide A+

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Test Bank For Pathophysiology: A Practical Approach 5th Edition by Lachel Story, ISBN NO: 9781284288094| Complete Guide A+

Institution
Pathophysiology: A Practical Approach 5th E
Course
Pathophysiology: A Practical Approach 5th E











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Institution
Pathophysiology: A Practical Approach 5th E
Course
Pathophysiology: A Practical Approach 5th E

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Uploaded on
June 13, 2025
Number of pages
104
Written in
2024/2025
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Exam (elaborations)
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,Chapter 1 Cellular Function
a1 a1 a1


a1 1. An increase in cardiac size and function due to increased workload is termed
a1 a1 a1 a1 a1 a1 a1 a1 a1 a1 a1 a1 a1


A) Atrophy.
B) Functional.
C) Hypertrophy.
D) Inflammation.


a1 2. While assessing a patient diagnosed with Marfan's Syndrome, the nurse shouldinc
a1 a1 a1 a1 a1 a1 a1 a1 a1 a1 a1 1a


lude which of the following that is consistent with the syndrome?
a1 a1 a1 a1 a1 a1 a1 a1 a1 a1


A) Cardiac assessment for coarctation of the aorta.
a1 a1 a1 a1 a1 a1


B) Genital assessment for small testicles.
a1 a1 a1 a1


C) Mental assessment for impairment.
a1 a1 a1


D) Oral assessment for cleft palate.
a1 a1 a1 a1




a1 3. Children with PKU must avoid phenylalanine in the diet. Phenylalanine is mos
a1 a1 a1 a1 a1 a1 a1 a1 a1 a1 a1 a1


tlikely to be a component of
1a a1 a1 a1 a1 a1


A) Fat.
B) Sugar.
C) Protein.
D) Carbohydrate.


a1 4. A 17-year-old college-
a1 a1 a1


bound student receives a vaccine against an organism thatcauses meningitis. This
a1 a1 a1 a1 a1 a1 a1 a1 1a a1 a1 a1


is an example of
a1 a1 a1


A) primary prevention. a1


B) secondary prevention. a1


C) tertiary prevention. a1


D) disease treatment. a1




a1 5. Metaplasia is
a1 a1


A) The disorganization of cells into various sizes, shapes, and arrangements.
a1 a1 a1 a1 a1 a1 a1 a1 a1


B) The replacement of one differentiated cell type with another.
a1 a1 a1 a1 a1 a1 a1 a1


C) The transformation of a cell type to malignancy.
a1 a1 a1 a1 a1 a1 a1

,D) An irreversible cellular adaptation.
a1 a1 a1

, a1 6. During a routine ultrasound of a 38 year old women 26 weeks gestation reveals a
a1 a1 a1 a1 a1 a1 a1 a1 a1 a1 a1 a1 a1 a1 a1


fetus with a small square head, upward slant of the eyes, and low set ears. The
a1 a1 a1 a1 a1 a1 a1 a1 a1 a1 a1 a1 a1 a1 a1 a


nurse recognizes that these findings are consistent with which of the following
1 a1 a1 a1 a1 a1 a1 a1 a1 a1 a1 a1


?
A) Fragile X Syndrome. a1 a1


B) Monosomy X (Turner's Syndrome). a1 a1 a1


C) Trisomy 21 (Down's Syndrome).a1 a1 a1


D) Trisomy X (Klinefelter's Syndrome).
a1 a1 a1




a1 7. While discussing treatment options with a parent of a newly diagnosed Monoso
a1 a1 a1 a1 a1 a1 a1 a1 a1 a1 a1 a1


myX (Turner's Syndrome) child, the nurse should include which of the followin
1a a1 a1 a1 a1 a1 a1 a1 a1 a1 a1 a1


g?
A) There is no treatment or cure.
a1 a1 a1 a1 a1


B) Symptoms of the condition are treated with estrogen.
a1 a1 a1 a1 a1 a1 a1


C) Symptoms of the condition are treated with testosterone.
a1 a1 a1 a1 a1 a1 a1


D) Institutionalization is the preferred method of managing care. a1 a1 a1 a1 a1 a1 a1




a1 8. Which of the following assessment findings indicates an alteration in homeostatic
a1 a1 a1 a1 a1 a1 a1 a1 a1 a1 a1 1a


control mechanisms? a1


A) Fever
B) Throat pain a1


C) Joint stiffness
a1


D) Positive throat culture a1 a1




a1 9. What information should parents be given about the consequences ofphenylket
a1 a1 a1 a1 a1 a1 a1 a1 a1 a1 1a


onuria (PKU)? a1


A) Mental retardation is inevitable.
a1 a1 a1


B) PKU is commonly associated with other congenital anomalies.
a1 a1 a1 a1 a1 a1 a1


C) High dietary tyramine may help induce enzyme production.
a1 a1 a1 a1 a1 a1 a1


D) Failure to treat properly results in progressive mental retardation.
a1 a1 a1 a1 a1 a1 a1 a1




a1 10. Injury that occurs when blood flow is diminished to tissue is called
a1 a1 a1 a1 a1 a1 a1 a1 a1 a1 a1 a1 injury.
A) hypoxic
B) ischemic
C) hyperemic
D) neoplastic


a1 a1 11. Tay sachs is caused by which of the following?
a1 a1 a1 a1 a1 a1 a1 a1


A) A deficiency or absence of hexosaminidase A
a1 a1 a1 a1 a1 a1


B) A defect on chromosome 17 or 22
a1 a1 a1 a1 a1 a1


C) A mutation on chromosome 15
a1 a1 a1 a1

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