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Case Report

Rare Case of an Infant with Glutathione Synthetase Deficiency

Bassem Mohamad Abou Merhi, Sirine Mneimneh, Ahmad Shatila, Mariam Rajab.

An infant has generalized Glutathione Synthetase Deficiency. Pyroglutamic Aciduria (5-Oxoprolinuria) is a rare autosomal recessive disorder caused by either Glutathione Synthetase Deficiency or 5-Oxoprolinase Deficiency. The severe form of the disease, generalized GSSD, is characterized by acute Metabolic Acidosis, usually present in the neonatal period with Hemolytic Anemia and Progressive Encephalopathy.
We report a male infant who had a severe Metabolic Acidosis with high Anion Gap, Hemolytic Anemia, and Hyperbilirubinemia. High level of Pyruglutamic Acids was detected in his urine. He passed away of severe Metabolic Acidosis and Sepsis.

Key words: Glutathione Synthetase Deficiency. Newborn.

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Journal of Contemporary Medical Education


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