Sickle cell crisis can be prevented by avoiding fever, infection, acidosis, dehydration, constricting clothing, and exposure to cold.
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Q7: In a developing embryo, erythrocyte production shifts
Q8: Hemoglobin in a fetus has less affinity
Q9: Between 4 years of age and the
Q10: In beta-thalassemia major, most erythroblasts are destroyed
Q11: Erythroblastosis fetalis is defined as an:
A)allergic disease
Q13: How does HDN cause acquired congenital hemolytic
Q14: Rh incompatibility occurs in less than 10%
Q15: In a full-term infant, the normal erythrocyte
Q16: Sickled erythrocytes (characteristic of sickle cell anemia)
Q17: Fetal hemoglobin has a greater affinity for
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