GNRS 610 ADVANCED PATHOPHYSIOLOGY EXAM 2 HEMATOLOGY |
COMPLETE AND GRADED QUESTIONS AND ANSWERS 2026 LATEST
UPDATED | 100% GRADED CORRECT | 100% GUARANTEED TO PASS |
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Aplastic anemia is a serious anemia affecting pluripotential bone marrow stem cells and causing
all three hematopoietic cell lines to be reduced. What is the treatment for aplastic anemia in the
young and severely affected client?
a. There is no treatment for aplastic anemia
b. Bone marrow transplant
c. Spleen transplant
d. Liver transplant - (answer)b. Bone marrow transplant
Anemia of chronic inflammation is a mild to moderate anemia associated with chronic
infections, chronic noninfectious inflammatory diseases, and malignancies. Chronic diseases
which are common causes of this anemia include all of the following except:
a. Rheumatoid arthritis
b. AIDS
,c. Polycythemia vera
d. Systemic lupus erythematosus - (answer)c. Polycythemia vera
These conditions include AIDS, rheumatoid arthritis, systemic lupus erythematosus, malaria,
acute and chronic hepatitis, and chronic renal failure. This form of anemia also is commonly
noted in the presence of congestive heart failure.
Manifestations of chronic sickle cell disease in children include:
a. Atelectasis and pneumonia
b. Edema of the hands and feet
c. Stasis ulcers of the hands, ankles, and feet
d. Splenomegaly and hepatomegaly - (answer)c. Stasis ulcers of the hands, ankles, and feet
The manifestations of chronic sickle cell disease in children include stasis ulcers of the hands,
ankles, and feet
With time spleen may autoinfarct
Sickle cell disease (SCD) is inherited in an _____ fashion.
, a. Autosomal dominant
b. Autosomal recessive
c. X-linked dominant
d. X-linked recessive - (answer)b. Autosomal recessive
SCD is an inherited autosomal recessive disorder that is expressed as sickle cell anemia.
Sickle cell-thalassemia disease, and sickle cell-Hb C disease also occur.
Hemoglobin S (Hb S) is formed as a result of a(n):
a. Deficiency in G6PD that changes Hb A to Hb S
b. Genetic mutation in which two amino acids (histidine and leucine) are missing
c. Genetic mutation in which one amino acid (valine) replaces another (glutamic acid)
d. Autoimmune response in which one amino acid (proline) is detected as an antigen by
abnormal IgG - (answer)c. Genetic mutation in which a hydrophobic amino acid (valine)
replaces a hydrophilic amino acid (glutamic acid)
COMPLETE AND GRADED QUESTIONS AND ANSWERS 2026 LATEST
UPDATED | 100% GRADED CORRECT | 100% GUARANTEED TO PASS |
GET A+
Aplastic anemia is a serious anemia affecting pluripotential bone marrow stem cells and causing
all three hematopoietic cell lines to be reduced. What is the treatment for aplastic anemia in the
young and severely affected client?
a. There is no treatment for aplastic anemia
b. Bone marrow transplant
c. Spleen transplant
d. Liver transplant - (answer)b. Bone marrow transplant
Anemia of chronic inflammation is a mild to moderate anemia associated with chronic
infections, chronic noninfectious inflammatory diseases, and malignancies. Chronic diseases
which are common causes of this anemia include all of the following except:
a. Rheumatoid arthritis
b. AIDS
,c. Polycythemia vera
d. Systemic lupus erythematosus - (answer)c. Polycythemia vera
These conditions include AIDS, rheumatoid arthritis, systemic lupus erythematosus, malaria,
acute and chronic hepatitis, and chronic renal failure. This form of anemia also is commonly
noted in the presence of congestive heart failure.
Manifestations of chronic sickle cell disease in children include:
a. Atelectasis and pneumonia
b. Edema of the hands and feet
c. Stasis ulcers of the hands, ankles, and feet
d. Splenomegaly and hepatomegaly - (answer)c. Stasis ulcers of the hands, ankles, and feet
The manifestations of chronic sickle cell disease in children include stasis ulcers of the hands,
ankles, and feet
With time spleen may autoinfarct
Sickle cell disease (SCD) is inherited in an _____ fashion.
, a. Autosomal dominant
b. Autosomal recessive
c. X-linked dominant
d. X-linked recessive - (answer)b. Autosomal recessive
SCD is an inherited autosomal recessive disorder that is expressed as sickle cell anemia.
Sickle cell-thalassemia disease, and sickle cell-Hb C disease also occur.
Hemoglobin S (Hb S) is formed as a result of a(n):
a. Deficiency in G6PD that changes Hb A to Hb S
b. Genetic mutation in which two amino acids (histidine and leucine) are missing
c. Genetic mutation in which one amino acid (valine) replaces another (glutamic acid)
d. Autoimmune response in which one amino acid (proline) is detected as an antigen by
abnormal IgG - (answer)c. Genetic mutation in which a hydrophobic amino acid (valine)
replaces a hydrophilic amino acid (glutamic acid)
