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SICKLE CELL DISEASE

Sickle cell disease in Madhya Pradesh, Central India: A comparison of clinical profile of sickle cell homozygote vs. sickle-beta thalassaemia individuals

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Figures & data

Figure 1 Percent distribution of splenic status in SCD individuals representing non palpable splenomegaly and splenectomy in SCA, SBT, and total SCD groups

Figure 1 Percent distribution of splenic status in SCD individuals representing non palpable splenomegaly and splenectomy in SCA, SBT, and total SCD groups

Figure 2 Percent distribution of blood transfusions among three different groups (SCA, SBT, and Total SCD)

Figure 2 Percent distribution of blood transfusions among three different groups (SCA, SBT, and Total SCD)

Table 1 Common signs and symptoms observed in SCD patients

Table 2 Haematological profile of SCD patients

Table 3 Comparison of some clinical signs with foetal haemoglobin levels

Table 4 Age at first onset of clinical symptoms in SCD patients

Figure 3 Probable cause of death among SCD patients who died during the study period

Figure 3 Probable cause of death among SCD patients who died during the study period

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