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HKαα地中海贫血的基因诊断及临床表型分析
Chromosomal microarray analysis on fetues with ultrasound anomalies
【摘要】 目的对HKαα地中海贫血病例进行基因诊断,分析HKαα病例临床表型,为遗传咨询提供指导。方法对在本院就诊的HKαα病例进行血常规、血红蛋白电泳、基因诊断及产前诊断,分析病例的临床表型。结果共检测出HKαα病例33例,包括HKαα/αα15例、--SEA/HKαα16例、αWSα/HKαα1例、-α4.2/HKαα1例。并对5个家庭进行了产前诊断,检出--SEA/HKαα胎儿1例,通过遗传咨询,避免了选择性终止妊娠。结论结论 HKαα地中海贫血的基因诊断可以减少病例的漏诊或误诊,临床表型的分析可以为精准的遗传咨询提供指导。
【Abstract】 Objective To investigate the gene diagnosis and clinical presentation of HKααthalassemia and to provide an effective genetic counseling.Method Whole blood cell analysis,capillary zone electrophoresis(CZE),Gap-PCR and polymerase chain reaction-reverse dot blot(PCR-RDB)assay were performed to the HKααThalassemia,and analyze the hematological phenotype data of HKααThalassemia.Results 33 cases of HKααthalassemia were detected,including 15 cases of HKαα/αα、16 cases of --SEA/HKαα、1 case of αWSα/HKααand 1 case of -α4.2/HKαα.5 pedigrees were carried out prenatal diagnosis and 1 fetus of Hb --SEA/HKααwas detected.The couple choosed to continue the pregnancy.Conclusions Gene diagnosis of HKααthalassemia can make accurate diagnosis,avoiding the misdiagnosis.The analysis of HKααthalassemia clinical presentation can provide an effective genetic counseling.
- 【文献出处】 中国产前诊断杂志(电子版) ,Chinese Journal of Prenatal Diagnosis(Electronic Version) , 编辑部邮箱 ,2017年03期
- 【分类号】R714.5
- 【被引频次】4
- 【下载频次】187