Andersen ED, Krasilnikoff PA, Overvad H: Intermittent muscular weakness, extrasystoles, and multiple developmental anomalies. A new syndrome?
[karger.com]
RYR2, CASQ2, KCNJ2, ANK2, CALM1, CALM2, TRDN, SCN5A* Other Panels that Include this Diagnosis Notes on Genes: Priority Genes: These genes include >70% of the mutations that
[admerahealth.com]
Fainting spell 0001279 1%-4% of people have these symptoms Left ventricular dysfunction 0005162 Percent of people who have these symptoms is not available through HPO Autosomal
[rarediseases.info.nih.gov]