Genetic tests

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Full name	Analytes	Gene panels	Disease	Laboratory
Kennedy disease (Spinal and bulbar muscular atrophy, SBMA) - CAG repeat expansion	AR		Kennedy disease	Centrum Menselijke Erfelijkheid - KUL
Kennedy disease (Spinal and bulbar muscular atrophy, SBMA) - CAG repeat expansion	AR		Kennedy disease	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Kennedy disease (Spinal and bulbar muscular atrophy, SBMA) - CAG repeat expansion	AR		Kennedy disease	Centrum Medische Genetica - UZ Antwerpen
Kennedy disease / Spinal and bulbar muscular atrophy (SBMA) - AR gene CAG repeat expansion	AR		Kennedy disease	Centrum Medische Genetica - UZ Brussel VUB
Hypokalemic periodic paralysis, type 1 (CACNA1S gene hot spot mutations)	CACNA1S		Hypokalemic periodic paralysis	Centrum Medische Genetica - UZ Brussel VUB
Periodic paralysis (myotonia) / Paramyotonia congenita (SCN4A gene)	SCN4A		Hyperkalemic periodic paralysis, Hypokalemic periodic paralysis	Centrum Medische Genetica - UZ Brussel VUB
Arteriovenous malformation (gene panel)		Arteriovenous malformation (7 genes), Vascular malformations (germline) (38 genes) - UCL	Hereditary hemorrhagic telangiectasia, Heritable pulmonary arterial hypertension, Familial cerebral saccular aneurysm, Vein of Galen aneurysmal malformation, Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome, Capillary malformation-arteriovenous malformation, Parkes Weber syndrome, Microcephaly-capillary malformation syndrome	Centre de Génétique Médicale UCL