Hereditary Neuropathy Panel NeuroSeq

Synonyms

Allscripts (AEHR) Order Name

Hereditary Neuropathy Panel

Sunrise Clinical Manager (SCM) Order Name

Not Orderable

EPIC Order Name

Hereditary Neuropathy Panel

Clinical Info

Molecular confirmation of a clinical diagnosis
To assist with decisions about treatment and management of individuals with neuropathy
Testing of at-risk relatives for specific known mutation(s) previously identified in an affected family member 
  Prenatal diagnosis for known familial mutation(s) in at-risk pregnancies

Specimen Type

Blood

Container

Lavender Top Tube

Collection Instructions

Container/Tube:  Lavender top tube
Specimen: 2 - 5 mL whole blood
Transport Temperature: Room Temperature

Transport Instructions

Room Temperature

Specimen Stability

Methodology

Next-Gen Sequencing
Deletion/Duplication Analysis

Days Performed

Performing Laboratory

GeneDx

CPT

81448

PDM

1659921

Result Interpretation

See Report
 
Includes Genes:
AARS, ABHD12, AIFM1, ATL1, ATL3, ATP7A, BAG3, BICD2, BSCL2, CHCHD10, CNTNAP1, COX6A1, CYP27A1, DNAJB2, DNM2, DNMT1, DST, DYNC1H1, EGR2, ELP1, RETREG1, FBXO38, FGD4, FIG4, GAN, GARS, GDAP1, GJB1, GLA, GNB4, HADHA, HARS, HINT1, HSPB1, HSPB8, IGHMBP2, INF2, KARS, KIF1A, KIF5A, LITAF, LMNA, LRSAM1, MFN2, MME, MORC2, MPV17, MPZ, MTMR2, NDRG1, NEFH, NEFL, NGF, NTRK1, PDK3, PLEKHG5, PMP22, PNKP, PRDM12, PRPS1, PRX, RAB7A, REEP1, SBF1, SBF2, SCN11A, SCN9A, SCO2, SEPT9, SETX, SH3TC2, SIGMAR1, SLC12A6, SLC25A46, SLC52A2, SLC52A3, SLC5A7, SPG11, SPTLC1, SPTLC2, TFG, TRIM2, TRPV4, TTR, VAPB, VCP, VRK1, WNK1, YARS
 

Forms

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