Hereditary Persistence of Fetal Hemoglobin
Overview
Affiliations
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 after which only adult-type hemoglobin should be produced. The percentage of incorrect expression might be as low as 10%-15% or as high as 100% of the total hemoglobin, usually higher in homozygotes than in heterozygotes. The present case is a typical example of homozygous HPFH.
Homozygous Delta-Beta Thalassaemia With Alpha Thalassaemia and Erythrocytosis- a Rare Case Report.
Shokr H, Marwah M, Siddiqi H, Wright C, Marwah S Br J Biomed Sci. 2024; 81:13663.
PMID: 39640193 PMC: 11617142. DOI: 10.3389/bjbs.2024.13663.
Kerwash E, Sajic M, Rantell K, McBlane J, Johnston J, Niewiarowska A Curr Issues Mol Biol. 2024; 46(8):8209-8225.
PMID: 39194702 PMC: 11352399. DOI: 10.3390/cimb46080485.
Finotti A, Gambari R Front Genome Ed. 2023; 5:1204536.
PMID: 37529398 PMC: 10387548. DOI: 10.3389/fgeed.2023.1204536.
CRISPR-Cas9 base editors and their current role in human therapeutics.
Lahr W, Sipe C, Skeate J, Webber B, Moriarity B Cytotherapy. 2023; 25(3):270-276.
PMID: 36635153 PMC: 10887149. DOI: 10.1016/j.jcyt.2022.11.013.
Zurlo M, Nicoli F, Proietto D, Dallan B, Zuccato C, Cosenza L J Cell Mol Med. 2023; 27(3):353-364.
PMID: 36625233 PMC: 9889681. DOI: 10.1111/jcmm.17655.