Glutarazidurie Typ I, Diagnostik, Therapie und Management. S3-LL (DGKJ)

Publication Details

English Translation:

Diagnosis and management of glutaryl-CoA dehydrogenase deficiency.

Author(s):

• AWMF (DE) - Association of Scientific Medical Societies

Country(ies) of application:

• Germany

Language(s):

• German

Type of Publication:

Guideline

Primary Contact:

Ina Kopp
imwi@awmf.org

Publication URL:

Open Publication URL in a new window

Publication Scope:

• Assessment/diagnosis
• Management

Publication Status:

Published

Date of publication:

Oct 01, 2007

Due for Review:

Feb 29, 2016

Diseases / Conditions Addressed

MeSH Terms addressed:

• Nutritional and Metabolic Diseases (C18)
  • Metabolic Diseases (C18.452)
    • Glucose Metabolism Disorders (C18.452.394)
• Pediatrics (G02.403.776.610)

Associated Documentation

Associated Documentation:

• Group membership and declaration of interests
• Evidence tables (with a link to the evidence summary database if feasible)
• Consumer resources, patient version
• Short version
• Methodology / Development process

Additional Information

Long version of the guideline

Connect to existing guidelines of other professional societies:

Long version of the guideline: Konfirmationsdiagnostik bei Verdacht auf angeborene Stoffwechselkrankheiten aus dem Neugeborenenscreening

Guideline key questions