Clinical Trial: Review of French Cases of Glutathione Synthetase Deficiency

Study Status: Not yet recruiting
Recruit Status: Not yet recruiting
Study Type: Observational




Official Title:

Brief Summary: 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.