Category: Neurology

Krabbe Disease

Hereditary Spastic Paraplegia

Coenzyme Q10 Deficiency – Panel

Charcot-Marie-Tooth Disease, Demyelinating, Type 1a; CMT1A – Analysis by Oligo Array

Hereditary Neuropathy, with liability to pressure palsies; HNPP – Oligo Array

Cerebral Cavernous Malformations – Panel

Gaucher Syndrome

Fabry Disease

Alport Syndrome

Neurofibromatosis type 1