Galanello R, De Virgiliis S, Addis M, Paglietti E, Ruggeri R, Cao A
J Clin Pathol. 1980 Oct;33(10):946-8. doi: 10.1136/jcp.33.10.946.
We report red cell indices and haemoglobin (Hb)A2 levels in Sardinian children with heterozygous beta 0-thalassaemia and in normal controls aged 6 months to 12 years. Iron-deficient children and those with haematological findings indicative of alpha-thalassaemia were excluded. As in adult carriers, these subjects have significantly increased mean red cell counts and significantly reduced mean Hb levels, mean corpuscular volume (MCV), mean corpuscular haemoglobin (MCH), haematocrit, and mean corpuscular haemoglobin concentration. From 66 to 76% of the heterozygous beta 0 thalassaemia children examined were anaemic. MCH and MCV were within the normal range in 2.8% of these children. Serum ferritin levels showed no difference from those of normal controls.
我们报告了患有杂合子β0地中海贫血的撒丁岛儿童以及6个月至12岁正常对照儿童的红细胞指数和血红蛋白(Hb)A2水平。缺铁儿童以及那些有提示α地中海贫血血液学表现的儿童被排除在外。与成年携带者一样,这些受试者的平均红细胞计数显著增加,而平均血红蛋白水平、平均红细胞体积(MCV)、平均红细胞血红蛋白(MCH)、血细胞比容和平均红细胞血红蛋白浓度显著降低。接受检查的杂合子β0地中海贫血儿童中有66%至76%患有贫血。这些儿童中有2.8%的MCH和MCV在正常范围内。血清铁蛋白水平与正常对照无差异。