Abstract:
This study was hospital analytical, descriptive and cross-sectional conducted to
determine the sickle cell disease and sickle cell trait frequency in Sudanese patient in
Heglig area in Western of Southern Kordofan state in the period between November 2008
to February 2009.
One hundred (100) patients were informed about the study and agreement for
participation was obtained. A venous blood of 2.5 ml was collected in EDTA containers
and investigated for sickle cell disease and sickle cell trait, a complete blood count (CBC),
sickling test and haemoglobin electrophoresis were carried out.
Fully automated haematological analyzer (Sysmex Kx 21N), Electrophoresis tank
and power pack were used for analysis and statistical package for social sciences (SPSS)
computer program version 13 was used for data processing.
The mean age of the sickle cell disease patients was (7.92). The results showed
that percentage of sickle cell trait and sickle cell disease were (52) and (14) respectively.
The sickling test showed that (71%) of the study population were negative sickling test,
the remain (29%) were positive.
Haemoglobin level, total erythrocyte and packed cell volume of the sickle cell
disease patients were (6.59), (2.43) and (22.02), respectively.
There were no significant differences in sickle cell disease and normal individuals
in mean cell haemoglobin concentration (29.80), mean cell volume (92.50) and mean cell
haemoglobin (26.48) (p < 0.095, p < 0.226 and p < 0.400 respectively,
The total leukocytes (20.4) p < 0.000) and platelets count (280.78) p < 0.044) were
significantly elevated in sickle cell disease when compared with normal individuals.
In conclusion, sickle cell anaemia is highly frequent in the studied area, which is
most likely due to the consanguineous marriages.
