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A Rare Case of Abnormal Hemoglobin Variant Hb Mizuho: [ HBB : c.206T > C β 68(E12) Leu-Pro]: A First Report in the Chinese Population.

Ya-Ping ChenPeng WuHeng WangJiang-Fen WuDan XieLei WangBangquan AnShengwen Huang
Published in: Hemoglobin (2023)
A 6-month-old female infant presented with unexplained hemolytic anemia, showing no abnormalities by capillary electrophoresis and genetic testing for α- and β-thalassemia mutations that are commonly seen in the Chinese population. A rare Hb Mizuho: [ HBB : c.206T > C β 68(E12) Leu- Pro] variant was identified by next-generation sequencing (NGS) and verified by Sanger sequencing. Hb Mizuho: [ HBB : c.206T > C β 68(E12) Leu- Pro] is not easily detectable because it is extremely unstable, and the correct diagnosis is usually made via DNA sequencing. This is the first report of this variant in the Chinese population.
Keyphrases
  • rare case
  • capillary electrophoresis
  • anti inflammatory
  • circulating tumor
  • single cell
  • mass spectrometry
  • chronic kidney disease
  • single molecule
  • copy number
  • iron deficiency
  • genome wide
  • red blood cell