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Home > Locations & Services > Services > Pathology and Laboratory Medicine > Health Practitioners and the Laboratory > cytogeneticsneurologists

LeftTopContent Locations & Services Find:  Locations | Services Health Practitioners and the Laboratory Pathology and Laboratory Medicine HomeTest and Services CatalogueTransfusion Medicine Product CataloguePolicy and ProcedureJob AidsSpecimen Collection and TransportRequisitionsAntibiogramsGenetic Testing and Molecular GeneticsMicrobiology EssentialsTransfusion EssentialsReference RangesLaboratory SuppliesAcute Care SCM GuidelinesContact InformationPhysician Access to Patient Results eHR ViewerFor Physicians - SCM Opening A New Clinic LeftMiddleContent LeftBottomContent

PageTopContent Pathology and Laboratory Medicine Cytogenetics and Related Medical Genetics Essentials requisitions must be completed in full FloatingContent2Body ​Be sure to fill out the: Ordering physician name Clinic contact information Patient identifiction Ordering physician signature, where requested Incomplete requisitions will result in samples not being sent for testing. FloatingContent1 PageMiddleContent ​Cytogenetics and Related Medical Genetics Essentials Ordering Approvals Neurologists Lab Tests Cadasil Charcot-Marie-Tooth 1A (PMP22, MLPA only) Charcot-Marie-Tooth 1B (MPZ) Charcot-Marie-Tooth X-Linked (Cx32/GJB1) Duchene Muscular Dystrophy (DMD) Fascioscapulohumeral Muscular Dystrophy 1A (FSHMD1) Fragile X (FRAXA) Friedreich's Ataxia (FXN) Hereditary Neuropathy with Liability to Pressure Palsies (HNPP) (PMP22, MLPA only) Huntington Disease (HTT) - DIAGNOSIS ONLY, NOT FOR ASYMPTOMATIC PATIENTS/AT RISK FAMILY MEMBERS Limb-Girdle Muscular Dystrophy Types 2I, 2H (FKRP, TRIM332) Myotonic Dystrophy Type 1 (DMPK) Myotonic Dystrophy Type 2 (ZNF9) OPMD SCA1, SCA2, SCA3, SCA6, SCA7, SCA8, SCA17 Spinal Bulbar Muscular Atrophy (AR) Spinal Muscular Atrophy (SMN1) For these Lab Tests, use the Roy Romanow Provincial Laboratory Molecular Diagnostics – Molecular Genetics Requisition. PageBottomContent

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