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NSUN6 gene related symptoms and diseases

All the information presented here about the NSUN6 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,HGNC,NCBIGENE, Mendelian Rare Disease Search Engine.

Table of contents:

Top 5 symptoms and clinical features associated to NSUN6 gene

Symptoms // Phenotype % Cases
Tachycardia Very Common - Between 80% and 100% cases
Sudden cardiac death Very Common - Between 80% and 100% cases
Syncope Very Common - Between 80% and 100% cases
Atrial fibrillation Very Common - Between 80% and 100% cases
Myocardial infarction Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with NSUN6 gene alterations may also develop some of the following symptoms and phenotypes:

  • Commonly - More than 50% cases

  • Ventricular tachycardia
  • ST segment elevation
  • Shortened QT interval
  • Polymorphic ventricular tachycardia
  • Aborted sudden cardiac death

Rare diseases associated to NSUN6 gene

Here you will find a list of rare diseases related to the NSUN6. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


BRUGADA SYNDROME 4; BRGDA4

Description

Brugada syndrome is characterized by an ST segment elevation in the right precordial electrocardiogram leads (so-called type 1 ECG) and a high incidence of sudden death in patients with structurally normal hearts. The syndrome typically manifests during adulthood, with a mean age of sudden death of 41 +/- 15 years, but also occurs in infants and children (summary by Antzelevitch et al., 2005).For a discussion of the genetic heterogeneity in Brugada syndrome, see BRGDA1 (OMIM ).

Most common symptoms of BRUGADA SYNDROME 4; BRGDA4

  • Tachycardia
  • Sudden cardiac death
  • Syncope
  • Atrial fibrillation
  • Myocardial infarction


More info about BRUGADA SYNDROME 4; BRGDA4

SOURCES: OMIM MESH



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