MERRF
Clinical Genetic Test
Help
offered by
GTR Test Accession: Help GTR000501924.2
MITOCHONDRIAL DISEASEINHERITED DISEASEDYSMORPHOLOGY ... View more
Last updated in GTR: 2014-03-07
Last annual review date for the lab: 2024-03-13 LinkOut
At a Glance
Diagnosis
Inborn mitochondrial myopathy; Lethal infantile mitochondrial myopathy; MERRF syndrome more...
Genes (1): Help
MT-TK ()
Molecular Genetics - Sequence analysis of the entire coding region: Bi-directional Sanger Sequence Analysis
Not provided
Not provided
Not provided
Ordering Information
Offered by: Help
MGZ Medical Genetics Center
View lab's website
Informed consent required: Help
Decline to answer
Pre-test genetic counseling required: Help
Decline to answer
Post-test genetic counseling required: Help
Decline to answer
Recommended fields not provided:
Conditions Help
Total conditions: 4
Condition/Phenotype Identifier
Test Targets
Chromosomal regions/Mitochondria Help
Total chromosomal regions/mitochondria: 1
Chromosomal region/Mitochondrion Associated condition
Genes Help
Total genes: 1
Gene Associated Condition Germline or Somatic Allele (Lab-provided) Variant in NCBI
Methodology
Total methods: 1
Method Category Help
Test method Help
Instrument *
Sequence analysis of the entire coding region
Bi-directional Sanger Sequence Analysis
* Instrument: Not provided
Clinical Information
Test purpose: Help
Diagnosis
Recommended fields not provided:
Technical Information
Test Comments: Help
In addition quantitative analysis for determination of heteroplasmy
Availability: Help
Tests performed
Entire test performed in-house
Analytical Validity: Help
Sensitivity >98%, specifity >99%
Proficiency testing (PT):
Is proficiency testing performed for this test? Help
No
Recommended fields not provided:
Regulatory Approval
FDA Review: Help
Not provided
Additional Information

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