Neurology
Adult-onset Dystonia, Chorea or related movement disorder Panel
Overview
Test Name
Adult-onset Dystonia, Chorea or related movement disorder Panel
Test Code
NUE1003
Test Category
Gene Panels
Test Subcategory
Neurology
Disease(s) Targeted
Adult-onset dystonia, chorea or related movement disorder
Who Is The Test For?
Patients with a family history, clinical suspicion, or diagnosis of Dystonia, Chorea or related movement disorder with onset in adulthood.
Test Approach
Whole exome sequencing (WES) with in silico gene panel analysis.
No. of Genes
67
Panel Content
ACTB, AFG3L2, ANO3, APTX, ARSA, ATM, ATP13A2, ATP1A2, ATP1A3, ATP7B, C19orf12, CACNA1A, CHMP2B, CP, CSF1R, CYP27A1, DCAF17, DCTN1, DNAJC6, FBXO7, FTL, GBA1, GCH1, GFAP, GNAL, GRN, GTPBP2, HPCA, KMT2B, LRRK2, LYST, MAPT, MYORG, NKX2-1, PANK2, PARK7, PDGFB, PDGFRB, PINK1, PLA2G6, PNKD, PPP2R5D, PRKN, PRKRA, PRNP, PRRT2, RAB39B, RNF216, SGCE, SLC19A3, SLC20A2, SLC2A1, SLC30A10, SNCA, SPG11, SPR, SYNJ1, TBK1, THAP1, TIMM8A, TOR1A, TUBB4A, VPS13A, VPS16, VPS35, WDR45, XPR1
Deliverables
Clinical Report (Download a sample report here)
Turnaround Time
~3-6 weeks*
Specimen Requirements
For detailed information about the sample requirements, please consult our clinical sample requirements page.
About Adult-onset dystonia, chorea or related movement disorder
Adult-onset dystonia, chorea, and related movement disorders are neurological conditions that cause involuntary muscle contractions or abnormal movements, often linked to genetic changes.
Gene Panel Workflow
Order a test using our clinical portal
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