Cori-Forbes disease (GSD III)
Enzyme or protein defect
Glycogen debranching enzyme
Accumulates or becomes deficient
Limit dextrin
Key features
Milder than GSD I; normal lactate, hepatomegaly, myopathy
Management
High-protein diet, frequent feeds
Not clinical guidance. Written from standard clinical biochemistry, not from the uploaded documents, and marked unreviewed. Teaching-level reference for study and database seeding only. It must not be used to manage a patient.
Recent literature
Europe PMC · from cache · sorted by publication date
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1
Cardiomyopathy in glycogen storage diseases: diagnosis, prognosis, and advanced management.
Patel U, Gunes E, Chawla A, Ashman K, Taub A, Arakelyan T, Madani A, Patel K, Bui Q, Adler E. · 2026-07-10
unreviewed -
2
Metabolic Myopathies and HyperCKemia in Adulthood: A Clinical Approach to Diagnosis and Management
Shakerdi L. · 2026-03-01
open access unreviewed -
3
Non-specificity of symptoms in infantile-onset Pompe disease may delay the diagnosis and institution of treatment.
Senarathne UD, Jasinge E, Viknarajah Mohan S, Waidyanatha S. · 2022-03-09
cited 2× open access unreviewed -
4
251st ENMC international workshop: Polyglucosan storage myopathies 13-15 December 2019, Hoofddorp, the Netherlands.
Laforêt P, Oldfors A, Malfatti E, Vissing J, ENMC 251st workshop study group. · 2021-01-23
cited 6× unreviewed -
5
Biomarkers in Glycogen Storage Diseases: An Update.
Molares-Vila A, Corbalán-Rivas A, Carnero-Gregorio M, González-Cespón JL, Rodríguez-Cerdeira C. · 2021-04-22
cited 25× open access unreviewed -
6
Glycogen metabolism in humans.
Adeva-Andany MM, González-Lucán M, Donapetry-García C, Fernández-Fernández C, Ameneiros-Rodríguez E. · 2016-02-27
cited 339× open access unreviewed -
7
An insight into the biochemistry of inborn errors of metabolism for a clinical neurologist.
Christopher R, Sankaran BP. · 2008-04-01
cited 9× open access unreviewed
External claims. These come from an index outside this database and are not checked against it. Treat them as leads.