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地中海贫血是血红蛋白遗传性缺陷,使红细胞寿命明显缩短而引起的一种液血性贫血。近来有关本病的报导逐渐增多。我科于1977年开展了血红蛋白电泳技术,在短短二、三个月中即发现十多例,有10例患者均曾被误诊为其他疾病,其中1例曾被误诊达二十多年,现简介如下: (一)10例确诊前后之诊断(附表) (二)误诊的原因
Thalassemia is a hemolytic anemia that causes hereditary defects in hemoglobin, resulting in a marked reduction in the life span of red blood cells. Recent reports of this disease have gradually increased. Our department carried out the hemoglobin electrophoresis technology in 1977, in just two or three months that found more than 10 cases, 10 patients were misdiagnosed as other diseases, of which 1 had been misdiagnosed for more than 20 years, Are briefings are as follows: (A) 10 cases before and after diagnosis (Schedule) (B) misdiagnosis