Hereditary persistence of fetal hemoglobin (HPFH) is a condition with significant fetal hemoglobin (HbF) production which continues in adulthood. This is usually caused by mutations in the β- …

Hereditary Persistence of Fetal Hemoglobin (HPFH) is a rare benign asymptomatic genetic disorder where the HbF persists, and incidentally discovered on screening for other …

We studied 30 cases of HbS-HPFH (types 1 and 2), confirmed by molecular analysis, and report the haematological features and change in HbF levels over time.

2018年6月1日 · In this report we described a rare case of compound heterozygous mutation of South-East Asia type hereditary persistence of fetal hemoglobin (SEA-HPFH) and β …

THE "hereditary persistence of fetal hemoglobin" (HPFH) has received increasing attention since its first detection by Edington and Lehmann. 1 In this benign condition, the heterozygote has …

Hereditary persistence of fetal hemoglobin (HPFH) is a benign condition in which significant fetal hemoglobin production continues well into adulthood, disregarding the normal shutoff point …

遗传性持续性胎儿血红蛋白增高症 （ Hereditary persistence of fetal hemoglobin ， HPFH ）是成人红细胞中 持续存在过量的 胎儿血红蛋白 (Fetal hemoglobin ， Hb F) ，血液学检查正常的遗 …

This report describes a case of hereditary persistence of fetal hemoglobin (HPFH) presenting initially as a marginal placental abruption in a primiparous woman at 27 weeks gestation. …

2020年7月1日 · A new form of hereditary persistence of fetal hemoglobin (HPFH) producing 3%-8% Hb F in heterozygotes and an elevation of F-cell counts as measured by both the …

2014年11月14日 · Case: A 50 years male, father of a β-thalassemia major patient, reported having Fetal Hemoglobin, 94.90% without any symptoms while being investigated for his …