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Diseases » Brugada syndrome 1 » Summary
 

What is Brugada syndrome 1?

What is Brugada syndrome 1?

  • Brugada syndrome 1: A rare genetic disorder characterized by heart rhythm abnormalities which can result in sudden death if untreated. Type 1 is caused by a mutation in the SCN5A gene on chromosome 3p21. Symptoms most often occur during the night and the condition is most prevalent in Japan and Southeast Asia.

Brugada syndrome 1: Introduction

Types of Brugada syndrome 1:

Broader types of Brugada syndrome 1:

How serious is Brugada syndrome 1?

Complications of Brugada syndrome 1: see complications of Brugada syndrome 1

What causes Brugada syndrome 1?

Causes of Brugada syndrome 1: see causes of Brugada syndrome 1

What are the symptoms of Brugada syndrome 1?

Symptoms of Brugada syndrome 1: see symptoms of Brugada syndrome 1

Complications of Brugada syndrome 1: see complications of Brugada syndrome 1

Brugada syndrome 1: Testing

Diagnostic testing: see tests for Brugada syndrome 1.

Misdiagnosis: see misdiagnosis and Brugada syndrome 1.

How is it treated?

Doctors and Medical Specialists for Brugada syndrome 1: Medical Geneticist ; see also doctors and medical specialists for Brugada syndrome 1.
Treatments for Brugada syndrome 1: see treatments for Brugada syndrome 1

Name and Aliases of Brugada syndrome 1

Main name of condition: Brugada syndrome 1

Other names or spellings for Brugada syndrome 1:

sudden unexpected nocturnal death syndrome, SUNDS

 

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