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
