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Our patient was diagnosed with severe GSSD after neonatal onset, with symptoms including hemolytic anemia, hyperbilirubinemia and severe metabolic acidosis (intractable), urine-organic acid analysis results suggestive of the presence of 5-oxoprolinuria, and imaging results suggestive of central nervous system damage and developmental retardation in the infant at follow-up

These sites are in German so you might need Google Chrome or a translation app

J.StefanoniD.FuX.et al (2020)

This test kit can detect up to 14 G6PD gene mutations in one run and the results can be directly visualized as a precipitated dot on the membrane template to provide a readout of the patients G6PD allele

One type of these specialty cells is called killer T-cells