Related Experiment Video
Updated: Jun 9, 2026

Determining the Likelihood of Variant Pathogenicity Using Amino Acid-level Signal-to-Noise Analysis of Genetic Variation
Published on: January 16, 2019
Long QT Syndrome Type 5 With Coexisting KCNE1 and RYR2 Variants: A Diagnostic Ambiguity
Mohammad Hossein Nikoo1, Hossein Fatemian2, Amir Hossein Hassani2
1Non-Communicable Research Center Shiraz University of Medical Sciences Shiraz Iran.
Abstract:
Long QT syndrome (LQTS) predisposes to syncope and sudden cardiac death. Type 5 LQTS, linked to KCNE1 variants, is rare. A teenage female presented with recurrent syncope. ECG showed QTc 485 ms. Genetic testing identified KCNE1 and RYR2 variants. Beta-blockers and ICD prevented events. The case highlights diagnostic and genotype-phenotype challenges.
Related Concept Videos
Karyotyping
Karyotyping
Acute Coronary Syndrome III: Diagnostic Studies
Pleiotropy
Aneurysm II: Clinical Manifestations and Diagnostic Studies
Mitral Stenosis II: Clinical features and Diagnostic Tests

