neonatal glutathione synthetase deficiency

neonatal glutathione synthetase deficiency Frontiers Hemolytic Anemia Due to Gamma-Glutamylcysteine

Name: neonatal glutathione synthetase deficiency Frontiers Hemolytic Anemia Due to Gamma-Glutamylcysteine
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Hemolytic Anemia Due to Gamma Glutamylcysteine Synthetase Deficiency: A Rare Novel Case in an Arab Muslim Israeli Child Nineteen year follow up of a patient with severe glutathione synthetase deficiency Journal of Human Genetics Natural course of glutamine synthetase deficiency in a 3 year old patient ScienceDirect A rare case of Glutathione Synthetase Deficiency in a newborn with normal neurological development on follow up ScienceDirect Glutathione Participation in the Prevention of Cardiovascular Diseases Impaired Glutathione Synthesis in Neurodegeneration

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Maximov PY, Lee TM, Jordan VC

This intermediate undergoes three enzymatic steps catalyzed by phosphoglycerate dehydrogenase (PHGDH), phosphoserine aminotransferase 1 (PSAT1), and phosphoserine phosphatase (PSPH)

The most common adverse drug reactions (ADRs) associated with the FQs involve the gastrointestinal tract (nausea and diarrhoea), the central and peripheral nervous system (headache, dizziness, a pins and needles tingling or pricking sensation, confusion, hallucinations, and suicidal thoughts)