QUIZ ON ANEMIA | HEMATOLOGY QUIZ | MEDICAL QUIZ

Table of contents

QUES. 1 The highest reference ranges for hemoglobin, hematocrit, and RBC count is usually found

At birth

In boys older than 12 years of age

In girls older than 17 years of age

In both sexes between 1 and 5 years of age

Correct! Wrong!

QUES. 2 The following is not a feature of microcytic hypochromic anemia

Red blood cells smaller than normal

Reduced MCV and MCHC

Central pallor less than normal 1/3

It is due to decreased hemoglobin synthesis

Correct! Wrong!

QUES. 3 Iron deficiency anemia may develop in all the following conditions except

Billroth II operation

Colon Carcinoma

Hookworm infestation

Capillary hemangioma

Correct! Wrong!

QUES. 4 The substance in the diet which inhibits iron absorption is

Vitamin C

Tannate

Citric acid

Sugar

Correct! Wrong!

QUES. 5 The condition associated with increased demand of vitamin B12 is

Aplastic anemia

Splenectomy

Hypothyroidism

Pregnancy

Correct! Wrong!

QUES. 6 Vitamin B12-IF complex is absorbed in

First part of duodenum

Jejunum

Ileum

Second part of duodenum

Correct! Wrong!

QUES. 7 The intrinsic factor is required for the absorption of

Iron

Folic acid

Vitamin B12

Zinc

Correct! Wrong!

QUES. 8 The peripheral blood smear in Megaloblastic anemia shows following features except

Macroovalocytes

Hypersegmented neutrophils

Howell-Jolly bodies

Increased Reticulocytes

Correct! Wrong!

QUES. 9 The neutrophils in peripheral blood smear of megaloblastic anemia show

Howell-Jolly bodies

Hypersegmentation

Toxic granules in the cytoplasm

Shift to the left

Correct! Wrong!

QUES. 10 Following features are characteristic of intravascular red cell destruction except

Increased haptoglobin

Hemosiderinuria

Hemoglobinuria

Hemoglobinemia

Correct! Wrong!

QUES. 11 The feature indicative of extravascular red cell destruction is

Hemoglobinuria

Splenomegaly

Hemoglobinemia

Decreased haptoglobin

Correct! Wrong!

QUES. 12 Hemolytic anemia is characterized by all except

Thrombocytopenia

Increased reticulocytes

Erythroid hyperplasia

Increased erythropoietin levels

Correct! Wrong!

QUES. 13 Condition characterized by increased stercobilinogen in stool is

Aplastic anemia

Alcoholic liver disease

Complete biliary tract obstruction

Hemolytic anemia

Correct! Wrong!

QUES. 14 The peripheral blood in hereditary spherocytosis will show following features except

RBC without central pallor

High reticulocyte count

Increased MCV

Increased MCHC

Correct! Wrong!

QUES. 15 The hematological disorder benefited by splenectomy is

Hereditary spherocytosis

Sickle cell anemia

Thalassemia

Pernicious anemia

Correct! Wrong!

QUES. 16 The thalassemia syndrome is due to decreased or absence of synthesis of

α-globin chains

γ-globin chains

β-globin chains

Either α or β-globin chain

Correct! Wrong!

QUES. 17 Hydrops fetalis is fatal because

Hb Barts cannot deliver oxygen to tissues

The excess β-globin chains form insoluble precipitates

Microcytic red cells gets trapped in the placental blood vessels

HbH cannot bind to oxygen

Correct! Wrong!

QUES. 18 Hemoglobin electrophoresis in β-thalassemia major will reveal

Decreased HbA2

Decreased HbA

Increased HbH

Decreased HbF

Correct! Wrong!

QUES. 19 In sickle cell anemia replacement of the glutamic acid residue by a valine occurs at the 6th position of

β-globin chain

γ-globin chain

δ-globin chain

α-globin chain

Correct! Wrong!

QUES. 20 “Autosplenectomy” may develop in patients with

Hereditary spherocytosis

Sickle cell anemia

Thalassemia

Aplastic anemia

Correct! Wrong!

QUES. 21 The hemolytic anemia that does NOT produce splenomegaly is

Hereditary elliptocytosis

Thalassemia

Hereditary spherocytosis

Sickle cell anemia

Correct! Wrong!

QUES. 22 In sickling test, sickling is induced by

5% sodium chloride

3% sodium citrate

5% sodium trithionate

2% sodium metabisulphite

Correct! Wrong!

QUES. 23 Heinz bodies are found in

Thalassemia

Sickle cell anemia

Iron deficiency anemia

G6PD deficiency

Correct! Wrong!

QUES. 24 Hemolytic disease of the newborn develops with

Rh –ve fetus in an Rh +ve mother

Rh –ve fetus in an Rh –ve mother

Rh +ve fetus in an Rh +ve mother

Rh +ve fetus in an Rh –ve mother

Correct! Wrong!

QUES. 25 Paroxysmal nocturnal hemoglobinuria is

A congenital red cell disorder

An autoimmune disorder

Due to deficient synthesis of β-globin chain

An acquired mutational disorder of stem cell

Correct! Wrong!

QUIZ ON ANEMIA

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SAHIL BATRA

Hi, I’m the Founder and Developer of Paramedics World, a blog truly devoted to Paramedics. I am a Medical Lab Tech, a Web Developer and Bibliophiliac. My greatest hobby is to teach and motivate other peoples to do whatever they wanna do in life.

QUES. 1 The highest reference ranges for hemoglobin, hematocrit, and RBC count is usually found

QUES. 2 The following is not a feature of microcytic hypochromic anemia

QUES. 3 Iron deficiency anemia may develop in all the following conditions except

QUES. 4 The substance in the diet which inhibits iron absorption is

QUES. 5 The condition associated with increased demand of vitamin B12 is

QUES. 6 Vitamin B12-IF complex is absorbed in

QUES. 7 The intrinsic factor is required for the absorption of

QUES. 8 The peripheral blood smear in Megaloblastic anemia shows following features except

QUES. 9 The neutrophils in peripheral blood smear of megaloblastic anemia show

QUES. 10 Following features are characteristic of intravascular red cell destruction except

QUES. 11 The feature indicative of extravascular red cell destruction is

QUES. 12 Hemolytic anemia is characterized by all except

QUES. 13 Condition characterized by increased stercobilinogen in stool is

QUES. 14 The peripheral blood in hereditary spherocytosis will show following features except

QUES. 15 The hematological disorder benefited by splenectomy is

QUES. 16 The thalassemia syndrome is due to decreased or absence of synthesis of

QUES. 17 Hydrops fetalis is fatal because

QUES. 18 Hemoglobin electrophoresis in β-thalassemia major will reveal

QUES. 19 In sickle cell anemia replacement of the glutamic acid residue by a valine occurs at the 6th position of

QUES. 20 “Autosplenectomy” may develop in patients with

QUES. 21 The hemolytic anemia that does NOT produce splenomegaly is

QUES. 22 In sickling test, sickling is induced by

QUES. 23 Heinz bodies are found in

QUES. 24 Hemolytic disease of the newborn develops with

QUES. 25 Paroxysmal nocturnal hemoglobinuria is

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