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.
Detailed Summary:
Sponsor: University Hospital, Strasbourg, France
Current Primary Outcome: Immunologically determining human acid glutathione S-transferase in a human assay sample [ Time Frame: 1 hour after hospitalization ]
Original Primary Outcome: Same as current
Current Secondary Outcome:
Original Secondary Outcome:
Information By: University Hospital, Strasbourg, France
Dates:
Date Received: June 17, 2016
Date Started: July 2016
Date Completion: July 2017
Last Updated: July 8, 2016
Last Verified: January 2016