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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 &gt; C β 68(E12) Leu- Pro] variant was identified by next-generation sequencing (NGS) and verified by Sanger sequencing. Hb Mizuho: [ HBB : c.206T &gt; 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.

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