Brugada syndrome 5

Brugada syndrome 5 is a rare form of Brugada syndrome caused by a mutation in the SCN1B gene. This condition affects the heart's electrical system and is part of a group of disorders that can lead to abnormal heart rhythms. The definition of Brugada syndrome 5 emphasizes its genetic cause. People with this condition have a mutation in the SCN1B gene which is linked to heart conduction defects. Further details about its clinical features and presentation may require more specific study.

Information about symptoms is currently limited for this condition.

Brugada syndrome 5 is caused by mutations in the SCN1B gene. This genetic change affects how electrical signals travel through the heart, leading to a cardiac conduction defect that is characteristic of this form of Brugada syndrome.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

Information about research is currently limited for this condition.