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Article

Glycogen Storage Disease Because of a PRKAG2 Mutation Causing Severe Biventricular Hypertrophy and High-Grade Atrio-Ventricular Block.

Circulation. Heart failure - 1 Aug 2016

Yogasundaram Haran, Paterson Ian D, Graham Michelle, Sergi Consolato, Oudit Gavin Y

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Share to Adrenergic beta-Antagonists
Share to AMP-Activated Protein Kinases
Share to Atrioventricular Block

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cardiac Pacing, Artificial

Share to Defibrillators, Implantable

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Source

Identifiers

PMID: 27496753
DOI: 10.1161/CIRCHEARTFAILURE.116.003367

Genes

PRKAG2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Glycogen Storage Disease Because of a PRKAG2 Mutation Causing Severe Biventricular Hypertrophy and High-Grade Atrio-Ventricular Block.PMID 27496753Read ↗

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A new mutation in PRKAG2 gene causing hypertrophic cardiomyopathy with conduction system disease and muscular glycogenosis.Semantic proximity Read ↗

Cardiac manifestations of PRKAG2 mutation.Semantic proximity Read ↗

High prevalence of arrhythmic and myocardial complications in patients with cardiac glycogenosis due to PRKAG2 mutations.Semantic proximity Read ↗

PRKAG2 cardiac syndrome: familial ventricular preexcitation, conduction system disease, and cardiac hypertrophy.Semantic proximity Read ↗

PRKAG2 syndrome, a rare hypertrophic cardiomyopathy: a Brazilian long-term follow-up with extracardiac disorders.Semantic proximity Read ↗

Cardiac phenotype in glycogen storage disease type XV: a rare cardiomyopathy to bear in mind.Semantic proximity Read ↗

Genetic testing reveals PRKAG2 syndrome mimicking sarcomeric hypertrophic cardiomyopathy in an adolescent: a case reportSemantic proximity Read ↗

Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy.Semantic proximity Read ↗

PRKAG2 gene mutation indicating myocardial hypertrophy and Wolff-Parkinson-White syndrome in a 28-year-old woman.Semantic proximity Read ↗

Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathySemantic proximity Read ↗

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