Padmanabhan A, Thomas S, Sheth H, Venugopalan P
Department of Child Health, Ibra Central Hospital, Ibra, PO Box 03, PC 413, Sultanate of Oman.
Ann Trop Paediatr. 2001 Mar;21(1):45-9.
Iron deficiency is a common cause of microcytic anaemia. However, a high prevalence of haemoglobinopathies in the Arab population makes differential diagnosis difficult. This prospective study of anaemia in children attending a regional hospital in the Sultanate of Oman looked at the prevalence and causes of anaemia in 256 children, 153 in the age group 3-5 years (group A) and 103 in the age group 10-12 years (group B). Of the children studied, 45.1% in group A and 37.9% in group B were anaemic according to WHO criteria. All the anaemic children had low mean corpuscular haemoglobin and 75% showed microcytosis. Serum ferritin levels were normal and glucose-6-phosphate dehydrogenase deficiency did not contribute to the anaemia. The microcytosis and microcytic anaemia in the study population could be attributed to the alpha-thalassaemia trait which is highly prevalent in Oman. The information is of value in any country where there is a significant prevalence of alpha-thalassaemia genes because these can confound the diagnosis of iron deficiency.
缺铁是小细胞性贫血的常见病因。然而,阿拉伯人群中血红蛋白病的高患病率使得鉴别诊断变得困难。这项针对阿曼苏丹国一家地区医院儿童贫血情况的前瞻性研究,观察了256名儿童的贫血患病率及病因,其中153名儿童年龄在3至5岁(A组),103名儿童年龄在10至12岁(B组)。在所研究的儿童中,根据世界卫生组织标准,A组有45.1%的儿童贫血,B组有37.9%的儿童贫血。所有贫血儿童的平均红细胞血红蛋白含量均较低,75%表现为小红细胞症。血清铁蛋白水平正常,葡萄糖-6-磷酸脱氢酶缺乏并非导致贫血的原因。研究人群中的小红细胞症和小细胞性贫血可能归因于α地中海贫血特征,该特征在阿曼非常普遍。在任何α地中海贫血基因显著流行的国家,这些信息都很有价值,因为它们可能混淆缺铁的诊断。