A rare case of Andersen-Tawil Syndrome Type-1 with concealed clinical features

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A rare case of Andersen-Tawil Syndrome Type-1 with concealed clinical features

Session: Rare inherited cardiac conditions

Topic: Clinical

Speaker: Associate Professor B. Hunuk (Istanbul, TR)

Event: EHRA 2024

Congress Presentation

About the speaker

Associate Professor Burak Hunuk

Baskent University Istanbul Hospital , Istanbul (Türkiye)

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3 more presentations in this session

First documented clinical case of arrhythmogenic heterozygous TECRL variant

Speaker: Doctor A. Porretta (Lausanne, CH)

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A novel mutation in LIM domain-binding protein 3 (LDB3) responsible for cardiomyopathy in association with ventricular preexcitation and conduction abnormalities

Speaker: Doctor D. Siddharthan (New Delhi, IN)

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Genetically tailored therapy with flecainide for familial dilated cardiomyopathy

Speaker: Doctor J. Fernandez Sanchez (Granada, ES)

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Access the full session

Rare inherited cardiac conditions

Speakers: Associate Professor B. Hunuk, Doctor A. Porretta, Doctor D. Siddharthan, Doctor J. Fernandez Sanchez

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About the event

EHRA 2024

7 April - 9 April 2024

Sessions Presentations

Congress

A rare case of Andersen-Tawil Syndrome Type-1 with concealed clinical features

About the speaker

Associate Professor Burak Hunuk

3 more presentations in this session

First documented clinical case of arrhythmogenic heterozygous TECRL variant

A novel mutation in LIM domain-binding protein 3 (LDB3) responsible for cardiomyopathy in association with ventricular preexcitation and conduction abnormalities

Genetically tailored therapy with flecainide for familial dilated cardiomyopathy

Access the full session

Rare inherited cardiac conditions

About the event

EHRA 2024

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