Hemoglobin Flashcards
1
Q
What is the primary function of hemoglobin?
A
To transport oxygen from the lungs to the tissues and carbon dioxide from the tissues back to the lungs.
2
Q
True or False: Hemoglobin is a protein found in red blood cells.
A
True
3
Q
What is the structural unit of hemoglobin?
A
Hemoglobin is composed of four polypeptide chains, typically two alpha and two beta chains.
4
Q
Fill in the blank: Hemoglobin binds oxygen in the presence of _____ concentration.
A
high
5
Q
What are the heme groups in hemoglobin responsible for?
A
Binding to oxygen.
6
Q
Which molecule is released by hemoglobin when it delivers oxygen to tissues?
A
Carbon dioxide.
7
Q
True or False: The affinity of hemoglobin for oxygen decreases as pH decreases.
A
True
8
Q
What is the Bohr effect?
A
The physiological phenomenon where increased carbon dioxide and decreased pH reduce hemoglobin’s affinity for oxygen.
9
Q
What is the normal range of hemoglobin concentration in adult males?
A
13.8 to 17.2 grams per deciliter.
10
Q
Multiple Choice: What is the primary component of the heme group in hemoglobin? A) Iron B) Copper C) Zinc D) Magnesium
A
A) Iron
11
Q
Fill in the blank: Hemoglobin can exist in two forms: _____ and _____.
A
oxyhemoglobin, deoxyhemoglobin
12
Q
What condition is characterized by low levels of hemoglobin?
A
Anemia.
13
Q
True or False: Hemoglobin can carry carbon monoxide.
A
True
14
Q
What is methemoglobin?
A
A form of hemoglobin that is unable to bind oxygen due to the iron being in the ferric state.
15
Q
What role does 2,3-Bisphosphoglycerate (2,3-BPG) play in hemoglobin function?
A
It decreases hemoglobin’s affinity for oxygen, facilitating oxygen release to tissues.
16
Q
Multiple Choice: Which of the following conditions would likely increase hemoglobin levels? A) High altitude B) Anemia C) Chronic lung disease D) Hemorrhage
A
A) High altitude
17
Q
What is the main site of hemoglobin synthesis in the body?
A
Bone marrow.
18
Q
Fill in the blank: Hemoglobin consists of _____ heme groups.
A
four
19
Q
What is the difference between fetal hemoglobin and adult hemoglobin?
A
Fetal hemoglobin has a higher affinity for oxygen than adult hemoglobin.
20
Q
What is hemoglobin?
A
Hemoglobin is a protein in red blood cells responsible for transporting oxygen from the lungs to the rest of the body.
21
Q
True or False: Hemoglobin variants are structural changes in the hemoglobin molecule.
A
True
22
Q
What are the two main types of hemoglobin variants?
A
The two main types are inherited variants and acquired variants.
23
Q
Fill in the blank: The most common hemoglobin variant is _____ .
A
Hemoglobin S
24
Q
What condition is associated with Hemoglobin S?
A
Sickle cell disease
25
True or False: Hemoglobin A is the normal adult hemoglobin.
True
26
What is the primary difference between Hemoglobin A and Hemoglobin F?
Hemoglobin F (fetal hemoglobin) has a higher affinity for oxygen than Hemoglobin A.
27
Which hemoglobin variant is associated with alpha-thalassemia?
Hemoglobin H
28
What is the genetic basis for most hemoglobin variants?
Most hemoglobin variants are caused by mutations in the HBB gene on chromosome 11.
29
Multiple Choice: Which of the following is not a hemoglobin variant? A) Hemoglobin C B) Hemoglobin D C) Hemoglobin A D) Hemoglobin E
C) Hemoglobin A
30
What is the clinical significance of identifying hemoglobin variants?
Identifying hemoglobin variants can help diagnose and manage blood disorders.
31
True or False: Hemoglobin variants can only affect oxygen transport.
False
32
Fill in the blank: Hemoglobin _____ is known for causing increased resistance to malaria.
S
33
What is the function of Hemoglobin A2?
Hemoglobin A2 plays a role in oxygen transport and is a minor component of adult hemoglobin.
34
Multiple Choice: Which hemoglobin variant is most commonly found in people of African descent? A) Hemoglobin A B) Hemoglobin S C) Hemoglobin E D) Hemoglobin F
B) Hemoglobin S
35
What is the role of genetic testing in hemoglobin variant diagnosis?
Genetic testing can confirm the presence of specific hemoglobin variants and identify carriers.
36
True or False: Hemoglobin variants can be detected through electrophoresis.
True
37
What is the most severe clinical presentation of hemoglobin variants?
Sickle cell disease is often considered the most severe clinical presentation.
38
Fill in the blank: Hemoglobin _____ is associated with thalassemia.
F
39
What does the presence of Hemoglobin C indicate?
Hemoglobin C can indicate a mild form of hemolytic anemia.
40
Multiple Choice: Which hemoglobin variant is characterized by a mutation in the alpha-globin gene? A) Hemoglobin S B) Hemoglobin C C) Hemoglobin H D) Hemoglobin A
C) Hemoglobin H
41
What is the effect of hemoglobin variants on blood viscosity?
Some hemoglobin variants, like Hemoglobin S, can increase blood viscosity and lead to vaso-occlusive crises.
42
True or False: All hemoglobin variants are clinically significant.
False
43
What is the importance of prenatal screening for hemoglobin variants?
Prenatal screening can identify at-risk pregnancies and allow for early intervention.
44
Fill in the blank: Hemoglobin _____ is associated with chronic hypoxia and is common in people living at high altitudes.
F
45
What is the primary method used to separate and identify hemoglobin variants in the laboratory?
Hemoglobin electrophoresis
46
What is hemoglobin electrophoresis?
A laboratory technique used to separate different types of hemoglobin in a blood sample.
47
True or False: Hemoglobin electrophoresis can help diagnose sickle cell disease.
True
48
What does hemoglobin electrophoresis measure?
The relative amounts of various hemoglobin types in the blood.
49
Which hemoglobin variant is associated with sickle cell anemia?
Hemoglobin S (HbS)
50
Fill in the blank: Hemoglobin electrophoresis is typically performed on a sample of _____ .
blood
51
What is the purpose of using an electric current in hemoglobin electrophoresis?
To separate hemoglobin variants based on their charge and size.
52
Which hemoglobin variant is commonly found in individuals with thalassemia?
Hemoglobin F (HbF) and Hemoglobin A2 (HbA2)
53
True or False: Hemoglobin electrophoresis can differentiate between normal and abnormal hemoglobin types.
True
54
What is the main advantage of hemoglobin electrophoresis over other hemoglobin testing methods?
It provides a detailed profile of multiple hemoglobin types.
55
What is the primary sample type used for hemoglobin electrophoresis?
Whole blood or hemolysate.
56
Which technique is commonly used to visualize the results of hemoglobin electrophoresis?
Staining the gel after electrophoresis.
57
What is the significance of detecting Hemoglobin F in adults?
It may indicate a hematological disorder such as thalassemia or sickle cell disease.
58
Multiple choice: Which of the following is NOT a hemoglobin variant tested in electrophoresis? A) HbA B) HbS C) HbE D) HbA1c
D) HbA1c
59
Fill in the blank: The normal adult hemoglobin is primarily composed of _____ .
Hemoglobin A (HbA)
60
What is the typical migration pattern of Hemoglobin S in electrophoresis?
It migrates slower than Hemoglobin A.
61
True or False: Hemoglobin electrophoresis can be used to monitor treatment in patients with hemoglobin disorders.
True
62
What is the role of buffer in hemoglobin electrophoresis?
To maintain the pH and ionic strength during the electrophoresis process.
63
Which population is most likely to have Hemoglobin S?
Individuals of African descent.
64
Multiple choice: Which hemoglobin variant is associated with an increased risk of thromboembolism? A) HbA B) HbS C) HbC D) HbF
B) HbS
65
What is the clinical significance of identifying Hemoglobin C?
It can indicate a different type of hemoglobinopathy that may require specific management.
66
Fill in the blank: The primary use of hemoglobin electrophoresis in newborns is to screen for _____ .
sickle cell disease
67
What is the expected percentage of Hemoglobin A in a healthy adult?
Approximately 95-98%.
68
True or False: Hemoglobin electrophoresis can identify carriers of sickle cell trait.
True
69
What is the importance of identifying different hemoglobinopathies?
To provide appropriate management and genetic counseling.
70
What are hemoglobinopathies?
Inherited disorders affecting the structure or production of hemoglobin.
71
True or False: Amino acid substitutions in hemoglobin can alter its oxygen-carrying capacity.
True
72
What is the most common hemoglobinopathy?
Sickle cell disease.
73
Fill in the blank: Sickle cell disease is caused by a substitution of __________ for glutamic acid at the sixth position of the beta-globin chain.
valine
74
Which amino acid is substituted in beta-thalassemia?
This condition is generally due to a reduction in the production of beta-globin chains rather than a specific substitution.
75
What is the role of hemoglobin in the body?
To transport oxygen from the lungs to the tissues and return carbon dioxide from the tissues to the lungs.
76
Multiple choice: Which amino acid substitution is responsible for Hemoglobin C disease? A) Valine, B) Lysine, C) Glutamic acid, D) Aspartic acid
B) Lysine
77
True or False: All amino acid substitutions in hemoglobin lead to severe clinical symptoms.
False
78
What type of mutation causes hemoglobinopathies?
Point mutations in the globin genes.
79
Short answer: What is the consequence of the amino acid substitution in sickle cell disease?
It causes hemoglobin to polymerize under low oxygen conditions, leading to distorted red blood cells.
80
Fill in the blank: Hemoglobin variants can be classified as __________ or __________.
pathological; benign
81
What is the function of the beta-globin gene?
To encode the beta chain of hemoglobin.
82
Multiple choice: Which condition is characterized by a substitution of aspartic acid for valine? A) Sickle cell disease, B) Hemoglobin C disease, C) Hemoglobin E disease, D) Beta-thalassemia
C) Hemoglobin E disease
83
True or False: Hemoglobinopathies can be detected through standard blood tests.
True
84
Short answer: What is the primary method used to identify hemoglobin variants?
Hemoglobin electrophoresis.
85
What are the potential complications of sickle cell disease?
Pain crises, infections, acute chest syndrome, and stroke.
86
Fill in the blank: The substitution of __________ for glutamic acid in hemoglobin leads to sickle cell trait.
valine
87
Multiple choice: Which hemoglobin variant is associated with increased resistance to malaria? A) Hemoglobin S, B) Hemoglobin C, C) Hemoglobin E, D) All of the above
D) All of the above
88
What is the significance of amino acid substitutions in the context of evolutionary biology?
They can confer advantages such as resistance to certain diseases.
89
True or False: Hemoglobinopathies are solely caused by genetic factors.
False
90
Short answer: How can lifestyle choices impact the symptoms of hemoglobinopathies?
Hydration, avoiding extreme temperatures, and managing stress can help reduce symptoms.
91
Fill in the blank: Hemoglobin variants can be classified as either __________ or __________ based on their clinical significance.
functional; dysfunctional
92
What is the difference between sickle cell disease and sickle cell trait?
Sickle cell disease presents with symptoms, while sickle cell trait usually does not.
93
True or False: Genetic counseling is recommended for individuals with a family history of hemoglobinopathies.
True
94
Short answer: Why is it important to understand amino acid substitutions in hemoglobin?
To better diagnose, manage, and treat hemoglobinopathies and their complications.
95
What is thalassemia?
Thalassemia is a blood disorder characterized by the reduced production of hemoglobin.
96
True or False: Thalassemia is an inherited condition.
True
97
Fill in the blank: Thalassemia primarily affects the production of __________.
hemoglobin
98
What are the two main types of thalassemia?
Alpha thalassemia and beta thalassemia.
99
Multiple Choice: Which type of thalassemia is caused by mutations in the alpha-globin gene?
A) Alpha thalassemia
100
What is the most severe form of beta thalassemia called?
Beta thalassemia major (also known as Cooley's anemia).
101
True or False: Individuals with thalassemia usually have normal hemoglobin levels.
False
102
What are common symptoms of thalassemia?
Symptoms include fatigue, weakness, pale skin, and jaundice.
103
Fill in the blank: Thalassemia can lead to complications such as __________ overload.
iron
104
Multiple Choice: Which of the following is NOT a treatment for thalassemia?
C) Antibiotics
105
What is the role of blood transfusions in managing thalassemia?
They help to maintain hemoglobin levels and reduce symptoms.
106
True or False: Thalassemia can only occur in people of Mediterranean descent.
False
107
What is the genetic inheritance pattern of thalassemia?
Thalassemia is inherited in an autosomal recessive pattern.
108
Multiple Choice: Which test is commonly used to diagnose thalassemia?
B) Hemoglobin electrophoresis
109
What are the potential long-term complications of thalassemia?
Complications include heart disease, diabetes, and bone deformities.
110
Fill in the blank: Patients with thalassemia may require __________ therapy to manage iron overload.
chelation
111
What is the function of hemoglobin in the blood?
Hemoglobin carries oxygen from the lungs to the body's tissues.
112
True or False: Genetic counseling can be beneficial for families affected by thalassemia.
True
113
What lifestyle changes can help manage thalassemia symptoms?
A balanced diet, regular medical check-ups, and avoiding iron supplements.
114
Multiple Choice: Which population is most commonly affected by beta thalassemia?
A) Mediterranean descent
115
What is the significance of prenatal testing in thalassemia?
Prenatal testing can identify thalassemia in unborn children.
116
Fill in the blank: __________ can help improve the quality of life for individuals with thalassemia.
Supportive care
117
What is a common misconception about thalassemia?
That it is a rare disease; it is actually quite common in certain populations.
118
True or False: Bone marrow transplant is a potential cure for thalassemia.
True
119
What role does iron play in the body?
Iron is essential for the production of hemoglobin and oxygen transport.
120
Multiple Choice: Which of the following is a symptom of iron overload?
C) Joint pain
121
What is the purpose of regular monitoring in patients with thalassemia?
To assess hemoglobin levels and manage complications.
