NGS Fetale Herzrythmusstörungen (Kardiale Arrhythmien)

Zugehörige Erkrankungen:
Long-QT-Syndrom (LQTS)
Short-QT-Syndrom (SQTS)
Sick Sinus Syndrom (SSS)
Brugada-Syndrom (BrS)
Katecholaminerge polymorphe ventrikuläre Tachykardie (CPVT).

Long-QT-Syndrom (LQTS) Gen Panel (15 Gene)
AKAP9, ANK2, CACNA1C, CALM1, CAV3, KCNE1, KCNE2, KCNH2, KCNJ2, KCNJ5, KCNQ1, NOS1AP, SCN4B, SCN5A, SNTA1

Short-QT-Syndrom (LQTS) Gen Panel (3 Gene)
KCNH2, KCNQ1, KCNJ2

Brugada-Syndrom (BrS) Gen Panel (17 Gene)
CACNA1C, CACNA2D1, CACNB2, GPD1L, HCN4, KCND3, KCNE1L, KCNE3, KCNH2, KCNJ8, RANGRF, SCN1B, SCN2B, SCN3B, SCN5A, SSCN5A, TRPM4

Sick-Sinus-Syndrom Gen Panel (3 Gene)
HCN4, MYH6, SCN5A

Katecholaminerge polymorphe ventrikuläre Tachykardie (CPVT)
Gen Panel (3 Gene) RYR2, CASQ2, CALM1