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尼日利亚北部对血红蛋白病进行脐血筛查。

Cord blood screening for haemoglobinopathies in northern Nigeria.

作者信息

Kulkarni A G, Jekeme S D

出版信息

Ann Trop Med Parasitol. 1986 Oct;80(5):549-51. doi: 10.1080/00034983.1986.11812064.

Abstract

Seven hundred cord blood samples were screened for the presence of abnormal haemoglobins by haemoglobin electrophoresis using the cellulose acetate paper electrophoresis technique at pH 8.6. The commonest abnormal haemoglobin was haemoglobin S (HbS), which was detected in 158 (22.57%) samples of which 20 (2.85%) were homozygous. HbC was present in 16 (2.28%) samples 42 (6%) had a fast-moving haemoglobin (HbBarts), and an additional five had only foetal haemoglobin (HbF). The tribal and ethnic distribution of these abnormal haemoglobins was in line with that described earlier by other workers. Attempts to follow up the babies with homozygous HbS, HbC and HbF were not successful.

摘要

采用pH 8.6的醋酸纤维素纸电泳技术,通过血红蛋白电泳对700份脐血样本进行异常血红蛋白筛查。最常见的异常血红蛋白是血红蛋白S(HbS),在158份(22.57%)样本中检测到,其中20份(2.85%)为纯合子。16份(2.28%)样本中存在血红蛋白C(HbC),42份(6%)有快速移动的血红蛋白(HbBarts),另外5份只有胎儿血红蛋白(HbF)。这些异常血红蛋白的部落和种族分布与其他研究人员先前描述的一致。对纯合子HbS、HbC和HbF婴儿进行随访的尝试未成功。

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