Familial short QT syndrome

Disease Export to PDF
Name:
Familial short QT syndrome
Description:
A rare, genetic cardiac rhythm disease characterized by a short QTc interval on the surface electrocardiogram (ECG) with a high risk of syncope or sudden death due to malignant ventricular arrhythmia.
ORPHAcode:
51083
Synonyms:
SQTS
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14