The heterogeneity in clinical presentations in sickle cell disease (SCD) alters between crisis
and steady state phases. Considering the pathophysiology, it is crucial to establish a …

Sickle cell disease (SCD) is a hereditary blood disorder characterized by abnormal
hemoglobin, leading sickle shape of red blood cells. It has several vascular complications …

Background Reference intervals (RIs) are crucial for the interpretation of results and overall
patient management. Of note, there are no established reference values for haematological …

Background: Sickle cell disease is an autosomal recessive disease characterized by an
aberrant production of hemoglobin S (HbS). The disease's presentation and severity varied …

Vasoclusion crisis is a major cause of morbidity and mortality in patients with Sickle Cell
Anemia (SCA). There are currently a paucity of data on the hemogram response to …

Generally, most of the hematological and biochemical parameters in SCD patients are
different from that of the other population. Hence, the importance of laboratory reference …

Background Reference intervals (RIs) are crucial for the interpretation of results and overall
patient management. Of note, there are no established reference values for haematological …

Biochemical response to vascoclusive crisis were investigated among Sickle Cell Anemia
(SCA) patients in Enugu metropolis, Southeast Nigeria. A total of 156 subjects comprising 75 …