Test Entry - Detail

Mitochondrial Disorders


General
  Clinical Use: Genetic testing, differential diagnosis, and prenatal testing. Common mutations only.
  Availability: Samples are tested Monday-Friday.
Molecular Genetics reports are issued in hardcopy to requesting doctor only.
  Aliases/Synonyms: Chronic Progressive External Ophthalmoplegia (mtDNA),   CPEO (mtDNA),   Kearns-Sayre Syndrome (mtDNA),   KSS (mtDNA),   Leber Hereditary Optic Neuropathy (MT-ND1 / MT-ND4 / MT-ND4L / MT-ND6),   LHON (MT-ND1 / MT-ND4 / MT-ND4L / MT-ND6),   Maternally Inherited Leigh Syndrome (MT-ATP6),   MELAS (MT-TL1),   MERRF (MT-TK),   MILS (MT-ATP6),   Mitochondrial Encephalomyopathy with Lactic Acidosis and Stroke-like Episodes (MT-TL1),   Myoclonic Epilepsy Associated with Ragged Red Fibers (MT-TK),   Myoclonic Epilepsy with Ragged Red Fibers,   NARP (MT-ATP6),   Neurogenic Weakness with Ataxia and Retinitis Pigmentosa (MT-ATP6),  
  Code: GPXOM
  Handling Instructions (to laboratory): Send sample ambient.
  Hyperlink:
  Reference Interval:
Not Applicable


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


Processing Requirements
  Alternate Containers:
  Processing Instructions: Store sample at room temperature.
  Minimum Assay Volume: 2mL
  Stability: 1 week 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 10:50