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Quiz on Human Pathophysiology

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Quiz on Human Pathophysiology
HCR240
Human Pathophysiology
Lesson 1 Quiz
This assignment is worth 40 points.
Please make sure you have answered all questions prior to submitting. Once you click the submit button, you will not be able to return.

Question

1 of 40
A 9-year-old patient is admitted to a pediatric unit with Duchenne muscular dystrophy. Which of the following traits was this condition inherited from? Sex-linked dominant Sex-influenced Sex-limited Sex-linked recessive
Question

2 of 40
A 70-year-old male with chronic renal failure presents with edema. Which of the following is the most likely cause of this condition? Increased capillary oncotic pressure Decreased interstitial oncotic pressure Increased capillary hydrostatic pressure Increased interstitial hydrostatic pressure
Question

3 of 40
Which of the following can cause swollen feet to develop? Increased ATP Chloride movement out of the cell Na+ movement into the cell Decreased oncotic pressure
Question

4 of 40
What is the role of cytokines in cell reproduction? Provide growth factor for tissue growth and development Block progress of cell reproduction through the cell cycle Restrain cell growth and development Provide nutrients for cell growth and development
Question

5 of 40
Sodium and water accumulation in an injured cell are a direct result of which of the following? Decreased ATP production Karyorrhexis Ribosome detachment Dehydration
Question

6 of 40
A cell that does not contain a multiple of 23 chromosomes is called a _____ cell. diploid euploid aneuploid haploid
Question

7 of 40
Which of the following molecules is likely to accumulate in dead or dying tissues? Calcium Protein Uric acid Melanin
Question

8 of 40
A condition in which a single chromosome is missing in each cell is called a haploid condition. an autosomy. a monosomy. Down Syndrome.
Question

9 of 40
A child is born with blue eyes (bb). The

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    Based on the description and symptoms given, the likely diagnosis would be Duchenne’s muscular dystrophy, or DMD; although DMD and its symptoms tend to show up at an earlier age but not always. This type of muscular dystrophy is the most common and severe form of the dystrophinopathic diseases. Dystrophinopathic diseases are muscular dystrophies that are of a genetic nature caused by a deficiency in the protein dystrophin. This protein is vital to muscle function and contraction. In the case of DMD, there is a mutation in the gene, called the DMD gene, responsible for producing dystrophin causing a deficiency. This gene mutation is X-linked recessive and is inherited. This means that females in the family carry the gene mutation and can pass is on to their offspring male or female, but it is expressed in the males.…

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