Test Entry - Detail


Charcot Marie Tooth Neuropathy (PMP22, MPZ, GJB1, MFN2)


General
  Clinical Use: Genetic testing, differential diagnosis, predictive testing and prenatal testing.
PMP22 analysis by MPLA and sequencing, MPZ and GJB1 bu sequencing of the shole coding region, MFN2 by partial screen only.
  Availability: Samples are tested Monday-Friday.
Patients must be referred by Genetic Services of WA: (08) 64581525.
Prenatal diagnosis must be arranged prior - please contact laboratory well in advance of sample collection date.
Molecular Genetics reports are issued in hardcopy to requesting doctor only.
  Aliases/Synonyms: CMT1,   CMT2,   CX32,   Dejerine Sottas Syndrome (PMP22, MPZ, GJB1, MFN2),   Hereditary Motor and Sensory Neuropathy (PMP22, MPZ, GJB1, MFN2),   Peripheral Neuropathy (PMP22, MPZ, GJB1, MFN2),  
  Code: DGS
  Handling Instructions (to laboratory): Send sample ambient.
  Hyperlink:
  Reference Interval:
Refer to report or laboratory


Collection Requirements
  Container: EDTA (LAV9),  
  Sample Type:
  Minimum Collection Volume: 2mL
  Collection Instructions:


Processing Requirements
  Alternate Containers:
EDTA (LAVENDER)
  Processing Instructions: Store sample at room temperature.
  Minimum Assay Volume: 2mL
  Stability: 7 days ambient
  Transport Instructions (to testing laboratory): Send sample ambient.


Testing Locations
  Performed at:
Section Department Site Contact Phone
Molecular Genetics Diagnostic Genomics QEII Medical Centre 6383 4243


Last Updated : 03-10-2020 10:16