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Thalassemia are characterized by:
A patient has the laboratory results shown in this table:
test |
result |
RBC |
6.5×106/μL(6.5×1012/L) |
HGB |
13.0g/dL(130 g/L) |
HCT |
39.0% |
MCV |
65μm3(65fL) |
MCH |
21.5pg |
MCHC |
33% |
These results are compatible with:
Laboratory findings in hereditary spherocytosis include:
Which of the following types of polycythemia is a severely burned patient most likely to have?
The characteristic morphologic feature in lead poisoning is:
The white cell feature most characteristic of pernicious anemia is:
Which parameter is most consistently abnormal in cases of hereditary spherocytosis?
What protein is commonly defective in hereditary elliptocytosis?
What is the most common mechanism resulting in hereditary stomatocytosis?
The basic mechanism associated with the development of sideroblastic anemia is:
Individuals with Fanconi anemia characteristically show:
Which of the following tumors are associated with erythrocytosis due to excessive erythropoietin production?
Which of the following features of G6PD deficiency are typically present on a Wright-Giemsa stained peripheral blood smear?
Which abnormal RBC morphology is associated with pyruvate kinase deficiency?
Which of the following hemoglobinopathies is associated with rod shaped crystals?
Which of the following statements about hemoglobin D and G is true?
This hemoglobinopathy results from a fusion product of the delta and beta gene:
Which of the following is consistent with the diagnosis of heterozygous beta-thalassemia?
Hereditary persistence of fetal hemoglobin (HPFH) is due to a loss of expression of this globin chain:
What is the specificity of cold auto agglutinin disease?