遗传性胎儿血红蛋白持续存在综合征是一种遗传性血液病。其特点是从出生到成年,红细胞内有高水平的HbF持续存在。此病在国内少见,1985年作者在Hb病普查中发现一例杂合子型并进行家系调查。先证者,女,53岁,壮族。平素健康,无自觉症状, Hereditary fetal hemoglobin persistence syndrome is a hereditary hematological disease. Its characteristic is from birth to adulthood, red blood cells have a high level of HbF persistence. The disease is rare in China. In 1985, the author found a case of heterozygote in the Hb disease census and conducted a pedigree investigation. Proof, female, 53 years old, Zhuang. Usually healthy, no symptoms,