| 1. | In the case of hemolytic anemia, PGK deficiency occurs in the erythrocytes.
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| 2. | Deficiency of gamma-glutamylcysteine synthetase in human is associated with enzymopathic hemolytic anemia.
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| 3. | The most common clinical manifestations are neonatal jaundice and acute hemolytic anemia.
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| 4. | It has not been associated with autoimmune hemolytic anemia of the fetus.
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| 5. | This includes : aplastic, posthemorrhagic, and hemolytic anemias and anemia of chronic disease.
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| 6. | In general, hemolytic anemia occurs as a modification of the RBC life cycle.
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| 7. | Aldolase A deficiency has been associated with myopathy and hemolytic anemia.
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| 8. | Individuals with cold agglutinin disease present with signs and symptoms of hemolytic anemia.
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| 9. | In autoimmune hemolytic anemia, concentrations of hemoglobin A1 ( HbA1 ) is undetectable.
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| 10. | Fortunately, apart from these episodes of hemolytic anemia, most G6PD-deficient individuals are entirely asymptomatic.
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