Search
long QT syndrome type 7 (Andersen syndrome, Andersen cardiodysrhythmic periodic paralysis, LQT7)
Genetics:
- associated with defects in KCNJ2
Clinical manifestations:
- clinical triad consisting of
a) K+-sensitive periodic paralysis
b) ventricular ectopy
c) dysmorphic features
Special laboratory:
- electrocardiogram
a) prolonged QT interval
b) ventricular ectopy
Interactions
disease interactions
Related
Jervell & Lange-Nielsen syndrome
General
long QT syndrome
Database Correlations
OMIM 170390