Symbol
| LQT9
|
Location
| 3p25
|
Name
|
long QT syndrome 9 |
Corresponding gene
|
CAV3
|
Main clinical features
|
prolonged QT interval and polymorphic ventricular arrhythmias (torsade de pointes); cardiac arrhythmias that may result in recurrent syncope, seizure, or sudden death |
Genetic determination
| not applicable |
Related entries
| . sudden infant death syndrome
|
Function/system disorder
| cardiovascular |
Type
| disease
|
Gene mutation | Chromosome rearrangement | Effect | Comments |
|
---|
various types
|  
| abnormal protein/gain of function
|  
| |