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  1. Article

    Open Access

    A Japanese neonatal case of glucose-6-phosphate dehydrogenase deficiency presenting as severe jaundice and hemolytic anemia without apparent trigger

    Glucose-6-phosphate dehydrogenase (G6PD) deficiency is rare among Japanese ethnicity although it is known as one of the most common hereditary disorders of erythrocytes, causing intravascular hemolysis. It is ...

    Shinya Tsuzuki, Moe Akahira-Azuma, Masao Kaneshige, Kazuhiro Shoya… in SpringerPlus (2013)

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