glutathione synthetase deficiency smear Diagnosis from the Blood Frontiers | Case report: A

Frontiers Case report: A Chinese patient with glutathione synthetase deficiency and a novel glutathione synthase mutation #imageoftheday, A 24 year old man develops acute jaundice and dark urine after starting trimethoprim sulfamethoxazole. A peripheral smear reveals the specific cellular defects shown. The underlying Glutathione Synthetase Deficiency as a Cause of Hereditary Hemolytic Disease New England Journal of Medicine Neuronal glutathione loss leads to neurodegeneration involving gasdermin activation Scientific Reports

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