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

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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

Session: Rare inherited cardiac conditions

Topic: Clinical

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

Event: EHRA 2024

Congress Presentation

About the speaker

Doctor Deepti Siddharthan

All India Institute of Medical Sciences (AIIMS), New Delhi (India)

3 presentations

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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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Video

Genetically tailored therapy with flecainide for familial dilated cardiomyopathy

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

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Slides

Video

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

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

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Slides

Video

Access the full session

Rare inherited cardiac conditions

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

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About the event

EHRA 2024

7 April - 9 April 2024

Sessions Presentations

Congress

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

About the speaker

Doctor Deepti Siddharthan

3 more presentations in this session

First documented clinical case of arrhythmogenic heterozygous TECRL variant

Genetically tailored therapy with flecainide for familial dilated cardiomyopathy

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

Access the full session

Rare inherited cardiac conditions

About the event

EHRA 2024

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