Clinical Profile of Sickle Cell Anaemia in Sudanese Children

dc.contributor.authorElawad Ahmed, Fataherahman
dc.contributor.authorOsman Gaboli, Hadia
dc.date.accessioned2018-08-15T18:03:42Z
dc.date.available2018-08-15T18:03:42Z
dc.date.issued2014-06
dc.description.abstractBackground: Although everyone with sickle cell anaemia shares a specific, invariant genotypic mutation, the clinical variability in the pattern and severity of disease manifestations is astounding. Objective:- To determine the clinical profile of sickle cell anaemia among Sudanese children. Patient and methods:- This was a cross-sectional hospital-based study of 100Sudanese children with sickle cell anaemia (SCA) age 5-15 years .It was conducted at the main tertiary children hospital in Sudan, between April-Augst2010 .The data was collected using a questionnaire that included medical history and clinical examination. Haemoglobin electrophoresis result was obtained from patients records.en_US
dc.identifier.issn1858-6155
dc.identifier.urihttp://hdl.handle.net/123456789/12547
dc.publisherneelain.edu.sden_US
dc.titleClinical Profile of Sickle Cell Anaemia in Sudanese Childrenen_US

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