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torsade-de-pointes syndrome with short coupling interval - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

torsade-de-pointes syndrome with short coupling interval

MONDO:0013317

Also known as:torsade DE pointes, short-coupled variant

Overview

Torsade-de-pointes (TdP) syndrome with short coupling interval is a very rare variant of Torsade de pointes, a polymorphic ventricular tachycardia, which is characterized by a short coupling interval of the first TdP beat on electrocardiogram in the absence of any structural heart disease. It manifests in early adulthood with syncope, often results in ventricular fibrillation and shows a high risk of sudden cardiac death.

ResearchLimited published research (4 articles)

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for torsade-de-pointes syndrome with short coupling interval.

4 publications have been identified in PubMed for torsade-de-pointes syndrome with short coupling interval. Research spans Case Report / Case Series (75%) and Basic Science / Preclinical (25%).

Recent Publications

Fiedler M (2026). [PMID: 41727060](https://pubmed.ncbi.nlm.nih.gov/41727060/). *bioRxiv : the preprint server for biology*. [Basic Science / Preclinical]
Sato A (2025). [PMID: 39602950](https://pubmed.ncbi.nlm.nih.gov/39602950/). *Journal of electrocardiology*. [Case Report / Case Series]
Dzebu AS (2025). [PMID: 40704271](https://pubmed.ncbi.nlm.nih.gov/40704271/). *Cureus*. [Case Report / Case Series]
Narasimha V V (2025). [PMID: 40653106](https://pubmed.ncbi.nlm.nih.gov/40653106/). *Indian pacing and electrophysiology journal*. [Case Report / Case Series]

Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 5:24 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:613600

Orphanet

European rare disease database

Orphanet:51084

GARD

Genetic and Rare Diseases Info Center

GARD:16651

Questions for Your Care Team

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torsade-de-pointes syndrome with short coupling interval

Overview

Research Landscape

Recent Publications

Medical References

External Resources

OMIM

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team