Atrial Standstill 2; Atrst2

Description

Atrial standstill (AS) is a rare condition characterized by the absence of electrical and mechanical activity in the atria. On surface ECG, AS is distinguished by bradycardia, junctional (usually narrow complex) escape rhythm, and absence of the P wave. Nearly 50% of patients with AS experience syncope. AS can be persistent or transient, and diffuse or partial (summary by Fazelifar et al., 2005).

Clinical Features

Top most frequent phenotypes and symptoms related to Atrial Standstill 2; Atrst2

  • Cardiomyopathy
  • Congestive heart failure
  • Dyspnea
  • Scarring
  • Stroke
  • Tachycardia
  • Tetraplegia
  • Syncope
  • Palpitations
  • Bradycardia

And another 5 symptoms. If you need more information about this disease we can help you.

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Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
No data available about the known clinical features onset.

Alternative names

Atrial Standstill 2; Atrst2 Is also known as cardiomyopathy, atrial dilated, with atrial standstill, atrial dilation and standstill.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.


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Atrial Standstill 2; Atrst2 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Atrial Fibrillation Panel.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center (United States).

SCN1B, SCN2B, SCN5A, SCN3B, GJA5, ABCC9, KCNA5, KCND3, KCNE1, KCNE2, KCNH2, KCNJ2, KCNQ1, LMNA, NPPA, NUP155
Specificity
7 %
Genes
100 %
NPPA.

By Institute for Human Genetics University Clinic Freiburg (Germany).

NPPA
Specificity
100 %
Genes
100 %
Cardiac Arrhythmia NGS Multi-Gene Panel (48 genes), Sequence & CNV analysis.

By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam (Netherlands).

RYR2, SCN10A, SCN1B, SCN2B, SCN4B, SCN5A, SNTA1, TNNT2, TRDN, CACNA1C, CACNA1D, CACNA2D1, CACNB2, CALM1, CALM2, CALM3, CASQ2, CAV3, SLMAP, HCN4 , (...)

View the complete list with 27 more genes
Specificity
3 %
Genes
100 %
Atrial fibrillation, familial 6 (sequence analysis of NPPA gene).

By CGC Genetics (Portugal).

NPPA
Specificity
100 %
Genes
100 %
Familial Atrial Fibrillation Syndrome Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

SCN1B, SCN2B, SCN5A, SCN3B, GJA5, ABCC9, KCNA5, KCND3, KCNE1, KCNE5, KCNE2, KCNH2, KCNJ2, KCNQ1, NPPA
Specificity
7 %
Genes
100 %
Atrial Fibrillation Syndrome via NPPA Gene Sequencing with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

NPPA
Specificity
100 %
Genes
100 %
Comprehensive Cardiology Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

RYR1, RYR2, SCN1B, SCN2B, SCN4B, SCN5A, SCO2, SGCD, SGCG, BRAF, SLC25A4, SNTA1, SOS1, SREBF2, TAZ, TBX3, TBX5, TCAP, TGFB2, TGFB3 , (...)

View the complete list with 143 more genes
Specificity
1 %
Genes
100 %
Comprehensive Cardiac Arrhythmia Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

RYR2, SCN10A, SCN1B, SCN2B, SCN4B, SCN5A, SNTA1, TGFB3, TNNI3, TRDN, CACNA1C, CACNA2D1, CACNB2, CALM1, CALM2, CALM3, CASQ2, CAV3, LDB3, SLMAP , (...)

View the complete list with 35 more genes
Specificity
2 %
Genes
100 %

We have 26 more panels available in our App

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Sources and references

You can check the following sources for additional information.

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