NGS Fetale Herzrythmusstörungen (Kardiale Arrhythmien)

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

Fetale Herzrythmusstörungen (gesamt) Gen Panel (32 Gene)
AKAP9, ANK2, CACNA1C, CACNA2D1, CACNB2, CALM1, CASQ2, CAV3, GPD1L, HCN4, KCND3, KCNE1, KCNE1L, KCNE2, KCNE3, KCNH2, KCNJ2, KCNJ5, KCNJ8, KCNQ1, MYH6, NOS1AP, RANGRF, RYR2, SCN1B, SCN2B, SCN3B, SCN4B, SCN5A, SNTA1, SSCN5A, TRPM4