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β°地中海贫血是由于β链合成受到完全抑制的一种遗传性疾病。其纯合予形成,国外已有报导,但国内仅见β°与β~+地中海贫血双重杂合子,纯合子患者尚未有报导。近2年夹在海南岛10万人的血红蛋白病普查中,我们发现3例β°地中海贫血纯合子。现报告如下: 例1 王××,女,16岁,黎族,万宁县人。1972年始感头晕、乏力,发热及面色苍黄,曾按肝炎,疟疾和钩虫病治疗,症状未见改善。1975年后未接受任
β ° Thalassemia is a hereditary disease that is completely inhibited by β-chain synthesis. Its homozygous to form, has been reported abroad, but the domestic only see β ° and β ~ + thalassemia heterozygotes, homozygous patients have not been reported. In the past two years, with a hemoglobin prevalence of 100,000 in Hainan Island, we found 3 homozygous β ° thalassemia. Now report as follows: Example 1 Wang × ×, female, 16 years old, Li, Wanning County. In 1972, it felt dizzy, weak, fever and pale yellow. It had been treated according to hepatitis, malaria and hookworm disease without any improvement in symptoms. After 1975 did not accept any appointment