LQT10

Jump to navigation Jump to search

Long QT Syndrome Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Long QT Syndrome from other Diseases

Epidemiology and Demographics

Risk Stratification

Screening

Natural History, Complications and Prognosis

Diagnosis

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

X-ray

CT scan

MRI

Other Imaging Findings

Other Diagnostic Studies

Genetic Studies

Treatment

Medical Therapy

Surgery

Primary Prevention

Secondary Prevention

Case Studies

Case #1

LQT10 On the Web

Most recent articles

Most cited articles

Review articles

Programs

slides

[1]

American Roentgen Ray Society Images of LQT10

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

on LQT10

CDC onLQT10

in the news

on LQT10

Directions to Hospitals Treating Long QT Syndrome

Risk calculators and risk factors for LQT10

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [2]

Overview

Only one mutation in one patient of this Long QT syndrome subtype has been found.

LQT10

Type OMIM Mutation
LQT10 SCN4B

This novel susceptibility gene for LQT is SCN4B encoding the protein NaVβ4, an auxiliary subunit to the pore-forming NaV1.5 (gene: SCN5A) subunit of the voltage-gated sodium channel of the heart. The mutation leads to a positive shift in inactivation of the sodium current, thus increasing sodium current. Only one mutation in one patient has so far been found.

References