最近我们在本地区进行血红蛋白病普查时发现一例遗传性胎儿血红蛋白持续综合征(HPFH),并作了家系调查。报告如下: 先证者唐×,男,39岁,汉族,广西南宁人,其祖籍是广东。患者平素健康,无贫血和黄疸病史,无任何自觉症状。查体:发育正常,营养尚 Recently, we found a case of hereditary fetal hemoglobin persistence syndrome (HPFH) at the time of the general survey of hemoglobin disease in our region and conducted a pedigree investigation. The report is as follows: Proofs Tang ×, male, 39 years old, Han nationality, Guangxi Nanning, whose ancestral home is Guangdong. Patients usually healthy, no history of anemia and jaundice, without any symptoms. Physical examination: normal development, nutrition is still