This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Genetics

Authoring team

Four genetic loci have been described which cause the hereditary long QT syndrome:

  • LQT1:
    • the KVLQT1 gene
    • codes for a potassium channel alpha subunit

  • LQT2:
    • the HERG gene
    • codes for a potassium channel subunit

  • LQT3:
    • the SCN5A gene
    • codes for a sodium channel subunit

  • LQT4:
    • no gene yet identified

Related pages

Create an account to add page annotations

Annotations allow you to add information to this page that would be handy to have on hand during a consultation. E.g. a website or number. This information will always show when you visit this page.