Jervell-lange Nielsen Syndrome

Overview of Jervell-lange Nielsen Syndrome

Most recent studies have shown that Jervell-lange Nielsen Syndrome shares some biological mechanisms with adams-stokes-syndrome, cardiac-arrest, cardiac-arrhythmia, cardiac-death, cardiac-fibrillation, complete-hearing-loss, congenital-heart-defects, deafness-congenital, heart-diseases, long-qt-syndrome, long-qt-syndrome-congenital, romano-ward-syndrome, sensorineural-hearing-loss-(disorder), sudden-cardiac-death, sudden-death, syncope, tachycardia-ventricular, torsades-de-pointes, ventricular-fibrillation.

Among the many pathways, these few ones have gauged particular interests from scientists studying Jervell-lange Nielsen Syndrome, and have been seen in publications frequently: Acid Secretion, Cardiac Conduction, Cellular Homeostasis, Gastric Acid Secretion, Ion Homeostasis, Ion Transport, Localization, Menopause, Pathogenesis, Secretion, Transport

Quite a number of genes have been found to play important roles in Jervell-lange Nielsen Syndrome, such as CAV3, COL18A1, ERG, GJB2, GJB6, KCNE1, KCNE2, KCNH2, KCNJ2, KCNQ1, MINK1, OXSM, RANGAP1, REST, RPS4Y1, RYR2, SCN5A, SLC17A5, UBN1. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.

In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.

Jervell-lange Nielsen Syndrome Related Genes

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Pathways Related to Jervell-lange Nielsen Syndrome

This information is being compiled and will come in a future update

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