Diagnostik, Therapie und Management der Glutarazidurie Typ 1 (Synonym: Glutaryl-CoA-Dehydrogenase-Defizienz). S3-LL (DGKJ)
- MeSH Terms
- Perinatology (H02.403.670.500); Nutritional and Metabolic Diseases (C18); Metabolic Diseases (C18.452); Glucose Metabolism Disorders (C18.452.394)
- Guideline Contact
- Ina Kopp (imwi@awmf.org)
- English Title Translation
- Diagnosis, therapy and management of glutaric aciduria type 1 (synonym: glutaryl-CoA dehydrogenase deficiency)
- Keywords
- Glutarazidurie Typ 1, Glutaryl-CoA-Dehydrogenase, Leitlinie, Management, Neugeborenenscreening, Therapie, Monitoring, Glutaric aciduria type I; glutaryl-CoA dehydrogenase; guideline; management; newborn screening; therapy; monitoring, acidurie glutarique, de type I, glutaryl-CoA déshydrogénase, directive actuelle, cadre du dépistage neonatal, traitement, Glutarik asidüri tip 1, Glutaril-KoA-dehidrojenaz enziminin, diyet, tedavi
- Date for Review
- 02/05/2027
- Publication Date
- 03/05/2022
- Publication Scope
- assessment
- management
- Countries of Application
- Germany
- Guideline Publication Status
- Published
- Languages
- German
- Authors
- AWMF (DE)
- Publication Year
- 2022