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Published: 10 septembre 2022 (3 semaines ago)

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We will refer to this as the « first post » or « first page ».A retrospective study of hematological, biochemical and anthropometric profile of children with sickle cell disease in Nigeria.
Sickle cell disease (SCD) is very common in Africans with about 100,000 afflicted children born every year, and is a leading cause of pediatric morbidity and mortality. This study was undertaken to determine the changes in hematological, biochemical and anthropometric profile of sickle cell disease patients in our environment. A retrospective review of the case records of children (Newborn to 15 years) with sickle cell disease treated at the University of Benin Teaching Hospital between June 1997 to June 2003 was done. Fifty-nine files were identified. Their mean age was 5.55 +/- 3.24 years with a median age of 4 years. The mean age of presentation was 2.78 +/- 2.47 years. Thirty-five (59%) of the patients were males and 24 (41%) were females. Sickle cell disease was the most common hemoglobinopathy among Nigerian children found in this study accounting for 25 (42.4%) of the cases. Sickle cell disease was the most common hemoglobinopathy, accounting for 25 (42.4%) of the cases, followed by α+ -thalassemia accounting for 16 (27.6%) of the cases. In most cases, both were present in 12 (20.7%). Sickle cell disease and Hb S- β(Thal) were the most common among the other causes of hemoglobinopathies. Short stature was common in the girls. Persistence of Hb F and reduced Hb A was common among Nigerian children with sickle cell disease. Co-existent elevation of aspartate aminotransferase (AST) level was also very common. More studies on the genotype and phenotype of other hemoglobinopathies in this environment are required.[A case of bronchial carcinoid of early stage with longitudinal grooved mu

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