Genetic tests

Full name Analytes Gene panels Disease Laboratory
Leber Congenital Amaurosis - Retinal dystrophy, early onset (gene panel) Leber Congenital Amaurosis - UGent Leber congenital amaurosis, Cone rod dystrophy, Retinitis pigmentosa, Senior-Loken syndrome, Severe early-childhood-onset retinal dystrophy Centrum Medische Genetica - UZ Gent
Diffuse gastric cancer, hereditary CDH1, CTNNA1 Hereditary diffuse gastric cancer Centrum Medische Genetica - UZ Gent
Diffuse gastric cancer (CDH1 gene) CDH1 Hereditary diffuse gastric cancer Centre de Génétique Humaine - CHU Sart-Tilman
Lissencephaly / subcortical band heterotopia PAFAH1B1 Lissencephaly due to LIS1 mutation, Subcortical band heterotopia Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Lissencephaly (LIS1 gene) PAFAH1B1 Lissencephaly due to LIS1 mutation Centrum Medische Genetica - UZ Brussel VUB
Malformations of cortical development (235 genes) Malformations of cortical development (235 genes) - VUB Bilateral perisylvian polymicrogyria, Cobblestone lissencephaly without muscular or ocular involvement, Lissencephaly due to LIS1 mutation, Lissencephaly due to TUBA1A mutation, Lissencephaly syndrome, Norman-Roberts type, Lissencephaly type 1 due to doublecortin gene mutation, Microlissencephaly, Polymicrogyria due to TUBB2B mutation, Subcortical band heterotopia, X-linked lissencephaly with abnormal genitalia Centrum Medische Genetica - UZ Brussel VUB
Long QT syndrome Long QT syndrome - UGent Brugada syndrome, Romano-Ward syndrome, Familial atrial fibrillation Centrum Medische Genetica - UZ Gent
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