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Assessment 1

Total questions: 10

Worksheet time: 7mins

Name
Class
Date
1.

Select the following that enhance Fe absorption (select all that apply) a. Citric acid b. Polyphenols (tea) c. Phytate (bran) d. Calcium e. Ascorbic acid

a)

Polyphenols (tea)

b)

Phytate (bran)

c)

Ascorbic acid

d)

Calcium

2.

Beta-thalassemia, unlike alpha-thalassemia, presents at approximately 6 months of age.

a)

True

b)

False

3.

Decreased or stopped production of alpha-globin chains results in HbH (4 gamma chains together) and Hb Barts (4 beta chains together)

a)

True

b)

False

4.

A 60 year old man presented with blackish stool for 2 days. He has underlying ischaemic heart disease on antiplatelet therapy. Clinically he is pale and not jaundice. His hemoglobin is 6 g/dL. What is the likely cause of his anaemia?

a)

Thalassemia

b)

Anaemic of chronic disease

c)

Iron deficiency anaemia

d)

autoimmune hemolytic anaemia

5.

A 15 year old girl presented with symptomatic anaemia. She has been regularly transfused monthly since the age of 6 months. However defaulted followup for the past 2 months. She is clinically pale and jaundice. Abdominal examination revealed hepatosplenomegaly. Her Hb is 4 g/dL. The likely diagnosis is

a)

Beta Thalassemia Major

b)

Beta Thalassemia trait

c)

Autoimmune Hemolytic Anaemia

d)

G6PD deficiency

6.

Hemolytic anaemia results in ________________ anaemia.

a)

Microcytic anaemia

b)

Normocytic anaemia

c)

Macrocytic anaemia

d)

None of the above

7.

When should you consider the diagnosis of hemolytic anaemia?

a)

Rapid drop of hemoglobin

b)

Presence of malaenic stool

c)

Increased in reticulocyte count

d)

None of the above

8.

Following are causes of immune hemolytic anaemia except

a)

Autoimmune hemolytic anaemia

b)

Paroxymal cold hemoglobinuria

c)

Thalassemia

d)

Hereditary spherocytosis

9.

List 4 (four) ways to classify hemolytic anaemia.

(a)  

10.

The following is/are the cause(s) of intravascular hemolysis

a)

Thalassemia

b)

G6PD deficiency

c)

Malaria

d)

Hereditary elliptocytosis