Genomic Unity® Movement Disorders Analysis

Movement disorders are a group of neurological conditions characterized by increased voluntary or involuntary movement or by decreased voluntary movement.

Genomic Unity® Movement Disorders Analysis is an effective test for the genetic cause of abnormal movement in patients with suspected diagnoses included within the following groups:

checkmarkAtaxias - a group of neurological conditions related to degeneration of the cerebellum, the area of the brain responsible for coordinating movement

checkmarkDystonias - a group of neurological conditions related to involuntary contraction of the muscles which causes repetitive or twisting movements

As well as suspected diagnoses of Parkinsons, Parkinsonism, Tyrosine hydroxylase deficiency and choreas including Hungtington disease and Huntington-like diseases.

Order this test when the patient presents with symptoms of impaired movement including ataxia, imbalance, gait disturbance, spasms and tremors and you'd like the option to reflex up to Genomic Unity® Exome  Plus Analysis.

checkmark Sequencing analysis of movement disorder-associated genes

checkmark Del/dup analysis of movement disorder-associated genes

checkmark Mitochondrial genome analysis with heteroplasmy (≥5%)

checkmark Adult-onset movement disorder (with or without cognitive involvement) STR analysis: AR, ATN1, ATXN1, ATXN2, ATXN3, ATXN7, ATXN8OS, ATXN10, C9ORF72, CACNA1A, CNBP, CSTB, DMPK, FMR1, FXN, PP2R2B

Optionally includes:

checkmark Huntington-related STR analysis (requires special consent): HTT, JPH3

checkmark Reflex to Genomic Unity™ Exome Plus Analysis

ABCB7, ABHD12, ABHD5, ACO2, ADAR, ADCY5, AFG3L2, AHI1, ALDH5A1, ANO10, ANO3, APTX, ARL13B, ARL6, ARSA, ATCAY, ATM, ATN1, ATP13A2, ATP1A3, ATP2B3, ATP7B, ATP8A2, ATXN1, ATXN10, ATXN2, ATXN3, ATXN7, ATXN8OS, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, BCAP31, BEAN1, CA8, CACNA1A, CACNA1B, CACNA1G, CACNB4, CAMTA1, CAPN1, CASK, CC2D2A, CCDC88C, CEP290, CEP41, CIZ1, CLCN2, CLN5, CLPP, COASY, COL6A3, COQ8A, COX20, CP, CPLANE1, CSTB, CWF19L1, CYP27A1, CYP2U1, DCAF17, DDC, DLAT, DNAJC19, DNAJC6, DNMT1, EBF3, EEF2, ELOVL4, ELOVL5, FA2H, FBXL4, FBXO7, FGF14, FLVCR1, FMR1, FTL, FXN, GBA2, GCDH, GCH1, GFAP, GLRA1, GNAO (GNOA1), GOSR2, GRID2, GRM1, GSS, HARS2, HEXA, HIBCH, HPCA, INPP5E, ITN2B, ITPR1, KCNA1, KCNC3, KCND3, KCNJ1, KCNMA1, KCTD17, KIF1C, KIF7, KMT2B, LAMA1, LARS2, LMNB1, LRPPRC, LRRK2, MAPT, MARS2, MECR, MKKS, MKS1, MME, MRE11, MTFMT, MTPAP, MTTP, NDUFAF6, NDUFS2, NDUFS4, NDUFS7, NDUFS8, NDUFV1, NKX2-1, NOL3, NPC1, NPC2, NPHP1, NUBPL, OFD1, OPA1, OPHN1, PANK2, PARK7, PDGFB, PDGFRB, PDYN, PEX7, PEX10, PHYH, PINK1, PLA2G6, PNKD, PNKP, PNPL86, POLG, POLR3A, POLR3B, PPP2R2B, PRKCG, PRKN, PRKRA, PRRT2, RELN, RNF216, RPGRIP1L, RUBCN, SACS, SCN2A, SCP2, SERAC1, SETX, SGCE, SIL1, SLC16A2, SLC19A3, SLC1A3, SLC20A2, SLC25A46, SLC2A1, SLC30A10, SLC52A2, SLC6A3, SLC9A6, SNCA, SNX14, SPG7, SPR, SPTBN2, STUB1, SYNE1, SYNJ1, SYT14, TAF1, TBP, TCTN1, TCTN2, TCTN3, TDP1, TGM6, TH, THAP1, TIMM8A, TMEM138, TMEM216, TMEM231, TMEM237, TMEM240, TMEM67, TOR1A, TOR1AIP1, TPK1, TPP1, TRAPPC11, TRIM32, TTBK2, TTC19, TTC8, TTPA, TUBB4A, TWNK, UBA5, VAMP1, VLDLR, VPS13A, VPS35, WDPCP, WDR45, WDR81, WFS1, WWOX, XPR1, ZFYVE26, ZNF423

Disorders that can be tested for include:

Ataxia with oculomotor apraxia
Ataxia with vitamin E deficiency
Ataxia-Telangiectasia, Ataxia-Telangiectasia-like disorder
Coenzyme Q10 deficiency
Dentatorubral-pallidoluysian atrophy (DRPLA)
Dopa-responsive dystonia
Episodic ataxia
Friedreich's ataxia
Huntington disease
Huntington disease like 2
Infantile onset ascending spastic paraplegia
Idiopathic torsion dystonia of mixed type
Marinesco-Sjogren syndrome
Mitochondrial recessive ataxia syndrome
Myoclonus-Dystonia
Parkinson’s disease, Parkinsonism
Posterior column ataxia with retinitis pigmentosa
Primary torsion dystonia
Spinocerebellar ataxia
Spastic ataxia
Tyrosine hydroxylase deficiency

81177x1, 81178x1, 81179x1, 81180x1, 81181x1, 81182x1, 81183x1, 81184x1, 81185x1, 81187x1, 81188x1, 81189x1, 81204x1, 81234x1, 81243x1, 81284x1, 81343x1, 81404x8, 81405x14, 81406x18, 81407x5, 81408x4, 81460x1, 81479x3 (81271x1, 81479x1)

The CPT codes provided are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.

Blood - 5ml
Saliva - contact us for a kit
gDNA - 5μg

Turn around time is ~8 weeks from sample receipt.


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