Inherited glutathione synthetase deficiency

MONDO:0017909

Glutathione synthetase deficiency is characterized by hemolytic anemia, associated with metabolic acidosis and 5-oxoprolinuria in moderate forms, and with progressive neurological symptoms and recurrent bacterial infections in the most severe forms.

Also known as: 5-oxoprolinuria, GSSD, glutathione synthetase deficiency, inborn error of glutathione synthase activity, inborn glutathione synthase activity disorder, inherited glutathione synthetase deficiency, pyroglutamic aciduria, pyroglutamicaciduria

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