Brugada syndrome 8

Brugada syndrome 8 is a form of Brugada syndrome where the cause of the condition is known to be a mutation in the HCN4 gene. Brugada syndrome refers to a range of heart rhythm disorders, and in this type, the genetic mutation in HCN4 leads to changes in the heart's electrical activity. This condition is identified as a rare disease, and being aware of the genetic cause helps in understanding the overall nature of the disorder. The focus on the HCN4 gene is important for distinguishing Brugada syndrome 8 from other types of Brugada syndrome.

Information about symptoms is currently limited for this condition.

Brugada syndrome 8 is caused by a mutation in the HCN4 gene. This mutation is the underlying reason for the changes in heart rhythm seen in this condition, differentiating it from other types 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.