The glutathione synthetase deficiency, inborn error of metabolism of autosomal recessive inheritance, is a rare disease (70 patients described in the world). The outcome of these patients and potential complications of this disease are not, to date, yet all known and described.
Study Type
OBSERVATIONAL
Enrollment
100
Service D'Urgences Medicales Pediatriques
Strasbourg, France
RECRUITINGImmunologically determining human acid glutathione S-transferase in a human assay sample
Time frame: 1 hour after hospitalization
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