Genetic Test Details

Neuromuscular Channelopathies Panel

Test Information

Titre
Neuromuscular Channelopathies Panel
Catégorie
Neurogenetics
Sub Category
Neuromuscular Disease
Gene/Platform/Region List
ATP1A2, CACNA1A, CACNA1S, CLCN1, KCNA1, KCNE3, KCNJ2, SCN4A, SLC12A3
Test type
Gene Panel
Samples Accepted
Blood, DNA
Indications
Carrier Cascade Testing, Diagnostics
Test Methodology
Sequencing
Disease/Condition
Neuromuscular Channelopathies, myotonia congenita, paramyotonia congenita, hyperkalemic periodic paralysis, hypokalemic periodic paralysis, Andersen-Tawil syndrome, potassium-aggravated myotonia

Dernière Mise à Jour: 05 septembre 2025