100% satisfaction guarantee Immediately available after payment Both online and in PDF No strings attached
logo-home
NR507/ NR 507 Midterm Exam (New 2024/ 2025 Update) Advanced Pathophysiology | Questions and Verified Answers| 100% Correct | A Grade – Chamberlain $11.49   Add to cart

Exam (elaborations)

NR507/ NR 507 Midterm Exam (New 2024/ 2025 Update) Advanced Pathophysiology | Questions and Verified Answers| 100% Correct | A Grade – Chamberlain

3 reviews
 246 views  7 purchases

NR507/ NR 507 Midterm Exam (New 2024/ 2025 Update) Advanced Pathophysiology | Questions and Verified Answers| 100% Correct | A Grade – Chamberlain QUESTION The patient with sickle cell anemia is at high risk for stroke Answer: True QUESTION Cells that contain abnormal t...

[Show more]

Preview 4 out of 32  pages

  • May 26, 2024
  • 32
  • 2023/2024
  • Exam (elaborations)
  • Questions & answers
  • nr 511 n
  • nr 5
All documents for this subject (36)

3  reviews

review-writer-avatar

By: johnkuehl • 9 hours ago

review-writer-avatar

By: michaelruffing • 1 month ago

review-writer-avatar

By: jesscarp8510 • 1 month ago

avatar-seller
ace_it
NR507/ NR 507 Midterm Exam (New 2024/
2025 Update) Advanced Pathophysiology |
Questions and Verified Answers| 100%
Correct | A Grade – Chamberlain
QUESTION
The patient with sickle cell anemia is at high risk for stroke


Answer:
True



QUESTION
Cells that contain abnormal types of hemoglobin are more susceptible to infection by the
parasite that causes malaria


Answer:
False



QUESTION
Which of the following statements are correct regarding thalassemia ?


Answer:
May have many possible genetic mutations



QUESTION
There are four genes involved in encoding synthesis of the alpha protein chains for Hb and are
located on chromosome number 16 .


Answer:
True

,QUESTION
The pathophysiology of sickle cell anemia involves a single amino - acid change on the beta -
chain


Answer:
True



QUESTION
Involves a single amino acid change on the beta - chain


Answer:
Sickle Cell Anemia



QUESTION
Increased red blood cell ( RBC ) hemoglobin S concentration , RBC dehydration , acidosis , and
hypoxemia


Answer:
Sickle Cell Anemia



QUESTION
May have many possible genetic mutations


Answer:
Thalassemia



QUESTION
Ineffective erythropoiesis

,Answer:
Thalassemia



QUESTION
Occurs primarily in persons from southeast Asia and China


Answer:
Thalassemia



QUESTION
Thalassemia is similar to sickle cell anemia in that the individual with thalassemia


Answer:
Inherits an abnormal Hb gene from both parents



QUESTION
Cells that contain abnormal types of hemoglobin are more susceptible to infection by the
parasite that causes malaria


Answer:
False



QUESTION
Sickle - cell anemia is an :


Answer:
Autosomal recessive genetic disorder .



QUESTION

, The patient with thalassemia is at high risk for stroke


Answer:
False



QUESTION
Sickle cell anemia and thalassemia are more prevalent in which of the following geographic
areas ?


Answer:
Africa .



QUESTION
Coronary artery disease ( CAD ) is mainly the result of :


Answer:
Longstanding atherosclerosis



QUESTION
Which of the following statements correctly describes the flow of blood between the heart and
lungs


Answer:
Oxygenated blood is transported from the lungs to the heart via the pulmonary veins



QUESTION
Which of the following is a modifiable risk factor for Coronary Artery Disease ( CAD ) ?


Answer:
Obesity

The benefits of buying summaries with Stuvia:

Guaranteed quality through customer reviews

Guaranteed quality through customer reviews

Stuvia customers have reviewed more than 700,000 summaries. This how you know that you are buying the best documents.

Quick and easy check-out

Quick and easy check-out

You can quickly pay through credit card or Stuvia-credit for the summaries. There is no membership needed.

Focus on what matters

Focus on what matters

Your fellow students write the study notes themselves, which is why the documents are always reliable and up-to-date. This ensures you quickly get to the core!

Frequently asked questions

What do I get when I buy this document?

You get a PDF, available immediately after your purchase. The purchased document is accessible anytime, anywhere and indefinitely through your profile.

Satisfaction guarantee: how does it work?

Our satisfaction guarantee ensures that you always find a study document that suits you well. You fill out a form, and our customer service team takes care of the rest.

Who am I buying these notes from?

Stuvia is a marketplace, so you are not buying this document from us, but from seller ace_it. Stuvia facilitates payment to the seller.

Will I be stuck with a subscription?

No, you only buy these notes for $11.49. You're not tied to anything after your purchase.

Can Stuvia be trusted?

4.6 stars on Google & Trustpilot (+1000 reviews)

73918 documents were sold in the last 30 days

Founded in 2010, the go-to place to buy study notes for 14 years now

Start selling
$11.49  7x  sold
  • (3)
  Add to cart