Andersen Syndrome

Overview of Andersen Syndrome

Most recent studies have shown that Andersen Syndrome shares some biological mechanisms with bidirectional-tachycardia, cardiac-arrhythmia, cardiac-death, channelopathies, familial-periodic-paralysis, hereditary-diseases, hypokalemic-periodic-paralysis, long-qt-syndrome, muscle-weakness, periodic-paralysis-(finding), polymorphic-ventricular-tachycardia, premature-ventricular-contractions, sudden-cardiac-death, sudden-death, tachycardia-ventricular, torsades-de-pointes, ventricular-arrhythmia, ventricular-tachycardia-catecholaminergic-polymorphic-1-(disorder), weakness.

Among the many pathways, these few ones have gauged particular interests from scientists studying Andersen Syndrome, and have been seen in publications frequently: Cardiac Conduction, Endocytosis, Lipid Binding, Localization, Membrane Depolarization, Myoblast Fusion, Pathogenesis, Swimming, Transport

Quite a number of genes have been found to play important roles in Andersen Syndrome, such as ABCA4, ANK2, CACNA1S, IKZF1, KCNE1, KCNE2, KCNH2, KCNJ12, KCNJ2, KCNJ4, KCNN4, KCNQ1, KIR3DL1, KRT1, SCN4A, SCN5A, SLC2A10. 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.

Andersen Syndrome Related Genes

click to see detail information for each gene

Pathways Related to Andersen Syndrome

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

Related Diseases