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Article

Phenotypic expression and clinical outcomes in a South Asian PRKAG2 cardiomyopathy cohort.

Scientific reports - 26 Nov 2020

Ahamed Hisham, Balegadde Aniketh Vijay, Menon Shilpa, Menon Ramesh, Ramachandran Aishwarya, Mathew Navin, Natarajan K U, Nair Indu Ramachandran, Kannan Rajesh, Shankar Meghna, Mathew Oommen K, Nguyen Thong T, Gupta Ravi, Stawiski Eric W, Ramprasad V L, Seshagiri Somasekar, Phalke Sameer

Abstract excerpt

The PRKAG2 syndrome is a rare autosomal dominant phenocopy of sarcomeric hypertrophic cardiomyopathy (HCM), characterized by ventricular pre-excitation, progressive conduction system disease and left ventricular hypertrophy. This study describes the phenotype, genotype and clinical outcomes of a South-Asian PRKAG2 cardiomyopathy cohort over a 7-year period. Clinical, electrocardiographic, echocardiographic, and...

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Identifiers

PMID: 33244021
DOI: 10.1038/s41598-020-77124-9
PMCID: PMC7691361

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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