Genetic tests

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Full name	Analytes	Gene panels	Disease	Laboratory
Craniosynostosis syndromes (Apert, Crouzon)	FGFR2		Crouzon syndrome, Apert syndrome	Centrum Medische Genetica - UZ Antwerpen
Craniosynostosis / Crouzon syndrome (hot spot mutation - exon 9)	FGFR3		Crouzon syndrome	Centre de Génétique Humaine - CHU Sart-Tilman
Charcot-Marie-Tooth type 1A / Hereditary Neuropathy with Liability to Pressure Palsies	PMP22		Charcot-Marie-Tooth disease type 1A, Hereditary neuropathy with liability to pressure palsies	Centrum Medische Genetica - UZ Gent
Charcot-Marie-Tooth type 1A (CMT1A) / Hereditary Neuropathy with Liability to Pressure Palsies	PMP22		Charcot-Marie-Tooth disease type 1A, Hereditary neuropathy with liability to pressure palsies	Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Charcot-Marie-Tooth type 1A / Hereditary Neuropathy with Liability to Pressure Palsies	PMP22		Charcot-Marie-Tooth disease type 1A, Hereditary neuropathy with liability to pressure palsies, Charcot-Marie-Tooth disease type 1E	Centrum Medische Genetica - UZ Antwerpen
Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)	PMP22		Charcot-Marie-Tooth disease type 1A, Hereditary neuropathy with liability to pressure palsies	Centre de Génétique Humaine - Erasme ULB
Charcot-Marie-Tooth type 1A (CMT1A) / Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)	PMP22		Charcot-Marie-Tooth disease type 1A, Dejerine-Sottas syndrome, Hereditary neuropathy with liability to pressure palsies	Centrum Menselijke Erfelijkheid - KUL
Charcot-Marie-Tooth type 1A / Hereditary Neuropathy with Liability to Pressure Palsies	PMP22		Charcot-Marie-Tooth disease type 1A, Hereditary neuropathy with liability to pressure palsies	Centre de Génétique Humaine - CHU Sart-Tilman
Charcot-Marie-Tooth (CMT1A, GJB1)	GJB1, PMP22		X-linked Charcot-Marie-Tooth disease type 1, Charcot-Marie-Tooth disease type 1A	Centre de Génétique Humaine - Erasme ULB

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