First report of an Asian family with hemoglobin Evans [α2 62 (E11) Val → Met]

Sae Ishimaru, Yuya Saito, Yuichi Yokokawa, Yuki Yuza, Takashi Kaneko

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)

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 languageEnglish
Pages (from-to)301-303
Number of pages3
JournalPediatrics International
Volume58
Issue number4
DOIs
Publication statusPublished - 1 Apr 2016
Externally publishedYes

Keywords

  • aplastic crisis
  • chronic hemolytic anemia
  • hemoglobin Evans
  • neonatal jaundice
  • unstable hemoglobin

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