Abstract
Hemoglobin Evans is an unstable variant caused by a single nucleotide mutation that produces a valine-to-methionine substitution at residue 62 of the α-globin chain. It has not been reported in the Asian population and only three cases have been reported worldwide. We diagnosed a Japanese boy with chronic hemolytic anemia with hemoglobin Evans after genetic testing. This is the first familial case of hemoglobin Evans in an Asian population.
Original language | English |
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Pages (from-to) | 301-303 |
Number of pages | 3 |
Journal | Pediatrics International |
Volume | 58 |
Issue number | 4 |
DOIs | |
Publication status | Published - 1 Apr 2016 |
Externally published | Yes |
Keywords
- aplastic crisis
- chronic hemolytic anemia
- hemoglobin Evans
- neonatal jaundice
- unstable hemoglobin