NGS Fetal heart arrhythmias

Fetal heart arrhythmias

Associated medical conditions:
Long-QT-Syndrome (LQTS)
Short-QT-Syndrome (SQTS)
Sick Sinus Syndrome (SSS)
Brugada-Syndrome (BrS)
Catecholaminergic polymorphic ventricular tachycardia (CPVT).

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

Short-QT-Syndrome (LQTS) Panel (3 genes)
KCNH2, KCNQ1, KCNJ2

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

Sick-Sinus-Syndrome Panel (3 genes)
HCN4, MYH6, SCN5A

Catecholaminergic polymorphic ventricular tachycardia (CPVT) Panel (3 genes)
RYR2, CASQ2, CALM1

Fetal heart arrhythmias (combined) Panel (32 genes)
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



  • How to order
    Order Form

    Place your order by email molekulargenetik@praenatal-medizin.de

  • Turnaround time
    2-3 weeks

  • Contact
    Priv.-Doz. Dr. med. M. Shoukier
    Dr. rer. nat. C. Bagowski molekulargenetik@praenatal-medizin.de

    Phone: +49 89 130744-0
    Fax: +49 89 130744-99

  • Ship the sample to our laboratory
    Material: DNA, Blood, Dried blood spot, Buccal swab, Chorionic villi (CVS), Amniotic fluid

    Shipping address:
    Pränatal-Medizin München
    Lachnerstr. 20
    80639 München
    Germany


  • Order specimen kit with sample tube, requisition form and prepaid return envelope by email.