Genetic tests

Full name Analytes Gene panels Disease Laboratory
Fukuyama congenital muscular dystrophy FKTN Congenital muscular dystrophy, Fukuyama type Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Retinoblastoma RB1 Hereditary retinoblastoma, Non-hereditary retinoblastoma Centrum Menselijke Erfelijkheid - KUL
Retinoblastoma RB1 Hereditary retinoblastoma, Non-hereditary retinoblastoma Centre de Génétique Médicale UCL
Hypophosphatasia ALPL Adult hypophosphatasia, Infantile hypophosphatasia, Odontohypophosphatasia, Perinatal lethal hypophosphatasia, Childhood-onset hypophosphatasia, Prenatal benign hypophosphatasia Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Inherited cardiac arrhytmia (gene panel) ANK2, CALM1, CASQ2, CAV3, KCNH2, KCNJ2, KCNQ1, RYR2, SCN5A, TRDN Inherited cardiac arrhytmia (25 genes) - IPG Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Primary Electrical disorders / Brugada syndrome / Long QT syndrome (LQT) / Short QT syndrome (SQT) / Arrhythmogenic right ventricular cardiomyopathy (ARVC) / Catecholaminergic polymorphic ventricular tachycardia (CPVT) (gene panel) ABCB4, ABCC9, ACTN2, AKAP9, ANK2, CACNA1C, CACNB2, CALM1, CALM2, CALM3, CASQ2, CAV3, CTNNA3, DES, DPP6, DSC2, DSG2, DSP, GJA1, GJA5, GPD1L, HCN4, JUP, KCNA5, KCND3, KCNE1, KCNE2, KCNE3, KCNE5, KCNH2, KCNJ2, KCNJ5, KCNJ8, KCNQ1, LMNA, NKX2-5, NOS1AP, NPPA, PKP2, PLN, PRKAG2, RANGRF, RYR2, SCN1B, SCN2B, SCN3B, SCN4B, SCN5A, SCN10A, SLMAP, SNTA1, TGFB3, TMEM43, TRDN, TRPM4, CACNA2D1, KCNK17, RRAD, PPA2, GNB5 Primary Electrical disorders/Brugada syndrome (genepanel) - UZA Centrum Medische Genetica - UZ Antwerpen
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