Genetic tests

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Full name	Analytes	Gene panels	Disease	Laboratory
Von Willebrand disease	VWF		Von Willebrand disease type 1, Von Willebrand disease type 2A, Von Willebrand disease type 2M, Von Willebrand disease type 2B, Von Willebrand disease type 2N, Von Willebrand disease type 3	Centrum Medische Genetica - UZ Antwerpen
Arterial Tortuosity Syndrome	SLC2A10, EFEMP2		Arterial tortuosity syndrome	Centrum Medische Genetica - UZ Gent
Porencephaly / Hemorrhagic stroke / Cerebral small vessel disease / Idiopathic cerebral white matter lesions / HANAC / Isolated retinal arteriolar tortuosity	COL4A1, COL4A2		Familial porencephaly, HANAC syndrome, Retinal arterial tortuosity	Centrum Medische Genetica - UZ Gent
Non Invasive Prenatal Testing (NIPT) of trisomies 13, 18 et 21 and sex chromosomes	Chromosome 21, Chromosome 13, Chromosome 18		Down syndrome, Trisomy 13, Trisomy 18	Centrum Menselijke Erfelijkheid - KUL
Non Invasive Prenatal Testing (NIPT) of trisomies 13, 18 et 21 and sex chromosomes	Chromosome 21, Chromosome 13, Chromosome 18		Down syndrome, Trisomy 13, Trisomy 18	Centrum Medische Genetica - UZ Gent
Non Invasive Prenatal Testing (NIPT) of trisomies 13, 18 et 21 and sex chromosomes	Chromosome 21, Chromosome 13, Chromosome 18		Down syndrome, Trisomy 13, Trisomy 18	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Non Invasive Prenatal Testing (NIPT) of trisomies 13, 18 et 21 and sex chromosomes	Chromosome 21, Chromosome 13, Chromosome 18			Centrum Medische Genetica - UZ Brussel VUB