Related Experiment Video
Updated: Jul 12, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Cardiomyopathy in glycogen storage diseases: diagnosis, prognosis, and advanced management
Umang Patel1, Eren Gunes1, Apaara Chawla1
1Division of Cardiovascular Medicine, University of California, San Diego, CA, USA.
Insights
Glycogen storage diseases (GSDs) cause inherited heart conditions with abnormal glycogen buildup. Early diagnosis and targeted therapies are crucial for managing these rare cardiomyopathies.
Area of Science:
- Cardiology
- Genetics
- Metabolic Disorders
Background:
- Glycogen storage diseases (GSDs) are rare inherited disorders.
- They lead to abnormal glycogen accumulation in tissues, including the heart.
- GSDs can mimic other heart conditions like hypertrophic cardiomyopathy.
Purpose of the Study:
- To review the spectrum of GSD-related cardiomyopathies.
- To discuss their pathophysiology, diagnosis, and treatment.
- To highlight the need for better evidence on specific therapies.
Main Methods:
- Literature review of GSDs and cardiomyopathy.
- Analysis of diagnostic approaches including imaging and genetic testing.
- Examination of current and emerging treatment strategies.
Main Results:
- GSDs present diverse cardiac phenotypes (hypertrophic, dilated, mixed).
- Key GSDs include Pompe, Danon, Cori, Andersen, Tarui, and others.
- Accurate diagnosis integrates clinical, imaging, and genetic data.
Conclusions:
- GSD cardiomyopathies require integrated diagnostic approaches.
- Specific treatments for GSD cardiomyopathies are still evolving.
- Further research is needed to develop targeted therapies for GSDs.
Abstract:
Glycogen storage diseases (GSDs) are a heterogeneous group of rare and often under-recognized causes of inherited cardiomyopathy characterized by pathological glycogen or autophagic vacuole accumulation of debris within various tissues, including the heart. These diseases often present as phenocopies of sarcomeric hypertrophic cardiomyopathy, though they may also manifest with dilated or mixed phenotypes. Key GSDs with cardiomyopathy include Pompe disease (GSD IIa), Danon disease (IIb), Cori/Forbes disease (GSD III), Andersen disease (GSD IV), Tarui disease (GSD VII), phosphorylase kinase deficiency (GSD IX), glycogenin-1 deficiency (GSD XV), and PRKAG2 syndrome, each presenting unique clinical trajectories. Accurate diagnosis requires integration of clinical red flags, multimodality cardiac imaging, and electrocardiography, alongside definitive diagnostic tools like enzyme screening, genetic testing, and endomyocardial biopsy. There is a dearth of evidence regarding specific treatment of each unique GSD cardiomyopathy, but emerging therapeutics across the spectrum of GSDs aim to address this need. This review covers current knowledge on the spectrum of GSD-related cardiomyopathies, discussing pathophysiology, diagnosis, and evolving treatment strategies.
Related Concept Videos
Cardiomyopathy V: Interprofessional Care
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Cardiomyopathy II: Dilated Cardiomyopathy
Cardiomyopathy VI: Nursing Management
Cardiomyopathy IV: Restrictive Cardiomyopathy
Cardiomyopathy I: Introduction and Classification
