The hemoglobin E thalassemias

Cold Spring Harbor Perspectives in Medicine
Suthat Fucharoen, David J Weatherall

Abstract

Hemoglobin E (HbE) is an extremely common structural hemoglobin variant that occurs at high frequencies throughout many Asian countries. It is a β-hemoglobin variant, which is produced at a slightly reduced rate and hence has the phenotype of a mild form of β thalassemia. Its interactions with different forms of α thalassemia result in a wide variety of clinical disorders, whereas its coinheritance with β thalassemia, a condition called hemoglobin E β thalassemia, is by far the most common severe form of β thalassemia in Asia and, globally, comprises approximately 50% of the clinically severe β-thalassemia disorders.

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Related Concepts

Adaptation, Physiological
Hemoglobin E
Genetic Carriers
Poly(A) Tail
5'-NUCLEOTIDASE
Alpha-Thalassemia
Thalassemia Minor
Nested Transcripts
Genome-Wide Association Study
Thalassemia

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