摘要
在1120例贫血原因待查者中,采用血红蛋白理化性质检查,诊断HbH病20例。遗传性HbH病16例中,Hb H3例,Hb H-Barts 8例、Hb H-G6PD缺陷症3例、HbH-Barts-G6PD缺陷症及HbH-MDS(RAEB)各1例;疑诊获得性HbH病4例中,Gaucher病-Hb H-Barts、AI-HA-Hb H-Barts,MDs(RAEB)-Hb H及MDS(RAEB-T)-Hb H各1例。湖北籍患者17例分布于本省11个市县。
The detection of physical and chemical properties of hemoglobin was performed in 1 120 cases. 20 cases were found to have HbH. Among 16 cases of hereditary HbH, 3 had HbH, 8 HbH-Barts, 3 Hb H-G6PD deficiency, one Hb H-Barts-G6PD deficiency and another one had Hb H-MDS (RAEB). 4 cases of suspected acquired Hb H had each Gaucher disease-Hb H, AIHA-Hb H-Barts, MDS (RAEB)-Hb H and MDS (RAEB-T)-HbH respectively. Among them 17 cases were distributed in 11 towns or counties in Hubei Province.
出处
《同济医科大学学报》
CAS
CSCD
北大核心
1991年第4期274-276,共3页
Acta Universitatis Medicinae Tongji
关键词
血红蛋白H病
诊断
α-thalassemia
hemoglobin H
hemoglobin Barts
