Familial ventricular tachycardia
Common Name(s)
Familial ventricular tachycardia
Advocacy and Support Organizations
Condition Specific Organizations
Following organizations serve the condition "Familial ventricular tachycardia" for support, advocacy or research.
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Advocacy and Support Organizations
Condition Specific Organizations
Following organizations serve the condition "Familial ventricular tachycardia" for support, advocacy or research.
Recommended Apps
Anonymously share and see how your answers compare with others with this condition while privately providing key pieces of information to medical researchers, disease advocacy groups, and others ONLY YOU select to help speed up cures and better alternatives.
Finding the right clinical trial for Familial ventricular tachycardia can be challenging. However, with TrialsFinder (which uses the Reg4ALL database and privacy controls by Private Access), you can permit researchers to let you know opportunities to consider - all without revealing your identity.
Scientific Literature
Articles from the PubMed Database
Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Familial ventricular tachycardia" returned 10 free, full-text research articles on human participants.
First 3 results:
Journal: Kardiol Pol. 2015 ;73(12):1339.
We report a three-generation family coming from southeastern region of Poland (Podkarpackie voivodship) with 6 women having normal hearts and presenting with a history of paroxysmal tachycardia with onset of symptoms in the adulthood. Recordings of clinical SVT, dual AVN electrophysiology, ...
Journal: Circ Arrhythm Electrophysiol. 2012 Aug;5(4):748-56.
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited arrhythmia syndrome associated with mutations in the cardiac ryanodine receptor gene (Ryr2) in the majority of patients. Previous studies of CPVT patients mainly involved probands, so current insight into ...
Journal:
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a severe inherited cardiac disorder caused by mutations predominantly in the ryanodine receptor (RyR2) gene. We sought to identify mutations in genes affecting cardiac calcium cycling in patients with CPVT and in less ...
To view other free, full-text articles on human participants, please click on the link below.
Reviews from the PubMed Database
Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Familial ventricular tachycardia" returned 0 free, full-text review articles on human participants.
No free, full-text review articles on human participants are available at this time. Please click this link to visit the PubMed website for results on "Familial ventricular tachycardia".
Symptoms, Diagnosis, and Treatment
https://ghr.nlm.nih.gov/gene/TMEM43
https://ghr.nlm.nih.gov/gene/TECRL
https://ghr.nlm.nih.gov/condition/wolff-parkinson-white-syndrome
https://ghr.nlm.nih.gov/gene/CALM2
https://ghr.nlm.nih.gov/gene/RYR2
https://ghr.nlm.nih.gov/condition/arrhythmogenic-right-ventricular-cardiomyopathy
https://ghr.nlm.nih.gov/condition/familial-hypertrophic-cardiomyopathy
https://ghr.nlm.nih.gov/condition/ankyrin-b-syndrome
https://ghr.nlm.nih.gov/gene/CASQ2
https://ghr.nlm.nih.gov/condition/left-ventricular-noncompaction
https://ghr.nlm.nih.gov/condition/jervell-and-lange-nielsen-syndrome
https://ghr.nlm.nih.gov/gene/MYBPC3
https://ghr.nlm.nih.gov/gene/CTNNA3
https://ghr.nlm.nih.gov/gene/MYL3
https://ghr.nlm.nih.gov/gene/DSG2
https://ghr.nlm.nih.gov/gene/KCNE5
https://ghr.nlm.nih.gov/gene/TNNT2
https://ghr.nlm.nih.gov/gene/HAND1
https://ghr.nlm.nih.gov/condition/familial-hypobetalipoproteinemia
There are currently no related results available in GeneReviews.
Clinical Trial Information This information is provided by ClinicalTrials.gov
There are currently no open clinical trials for this condition.

Finding the right clinical trial for Familial ventricular tachycardia can be challenging. However, with TrialsFinder (which uses the Reg4ALL database and privacy controls by Private Access), you can permit researchers to let you know opportunities to consider - all without revealing your identity.