In this study the demographic and clinical profile of 105 Yemeni children under 16 years old with sickle cell anemia (SCA) were studied. They were 53 males (50.4%) and 52 females (49.5%), aged between 0.5 and 15 years (mean 7.4ys). The most serious crisis as vaso-oclusive, hemolytic, sequestration and aplastic crisis were seen in (83.8%), (52.3%), (6.6%) and (5.7 %) respectively. The hand-foot syndrome was found in (21%) of all patients and in (51%) of children less than 3 years old. The most serious complication was the respiratory tract infections which was the most frequent in these patients, being encountered in (65.7%). The rate of hospitalization was of (76%). Our findings show that SCA has a severe clinical course in Yemenis, resembling that in black Africans and in black Americans.
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