Mitochondrial Encephalomyopathy: Lactic Acidosis (Stroke-like Episodes/MELAS)
Last updated: 29-DEC-11 PM | PDF View | Email Page
Test Code QA
Condition Description MELAS is characterized by mitochondrial encephalomyopathy, lactic acidosis, stroke-like episodes, often presenting in childhood. Other common symptoms include seizures, muscle weakness, recurrent headaches and vomiting, and exercise intolerance. Sensorineural hearing loss may also occur. Symptoms are highly variable, in part due to the amount of heteroplasmy (i.e., both normal and mutant mitochondrial DNAs are present in the same cell) and tissue distribution of abnormal mitochondria (replicative segregation). Symptoms may worsen during times of stress or illness.Mutations in the MTTL1 mitochondrial gene (tRNA-Leu) have been identified in patients with MELAS. Mutations in MTTL1 can result in impaired mitochondrial respiratory chain complex I and cytochrome C oxidase activity. Reduction in mitochondrial respiratory chain function reduces that amount of ATP produced by the mitochondria.The most common mutation in MTTL1, present in over 80% of patients with typical clinical findings of MELAS, is a 3243A>G transition in MTTL1. The MTTL1 mutations 3,271 T>C, 3,252 A>G, 3,291 T>C, and 3,260 A>G account for an additional 15-20% of all MELAS mutations. Other rare mutations in the MTTL1 gene have also been observed. Mitochondrial mutations outside the MTTL1 gene have been described in rare cases. Mutations associated with MELAS may be heteroplasmic with the degree of heteroplasmy varying in different tissues. Based on clinical presentation, either a blood or a tissue sample (muscle biopsy) may be used.References:
  • GeneReviews Clinical Summary
  • Patients with a confirmed or suspected diagnosis of MELAS.
  • Family members of an affected patient who are at risk for MELAS.
Related Tests
  • MERRF (QH) Testing may be indicated for patients who also show progressive external ophthalmaloplegia and ragged red fibers on muscle biopsy
  • KSS/CPEO (QB) Testing may be indicated for patients who also show progressive external ophthalmaloplegia
  • Myotonic Dystrophy (MD) may be indicated for patients who show muscle weakness
MethodologyThe MTTL1 mitochondrial gene (tRNA-Leu) is PCR amplified and sequenced in both the forward and reverse directions. The 3243A>G mutation is analyzed by a sensitive allele-specific extension assay to reliably detect heteroplasmic mutations. Patient gene sequences are compared to a normal reference sequence. Sequence variations are then classified as previously described mutations, novel mutations, or variations of unknown significance. This assay may detect variants of MTTL1 that may require further studies.
Reference RangesQualitative assay.
Special Instructions
DetectionThis assay will detect over 90% of mitochondrial mutations associated with MELAS. The 3243A>G mutation can be detected at approximately 10% heteroplasmy. All other mutations can be detected at approximately 15-20% heteroplasmy. Mutations outside the MTTL1 gene will not be detected.
Turnaround Time 3 weeks
Type Requirements Shipping
Whole BloodIn EDTA (purple top) or ACD (yellow top) tube:
Infants (<2 years): 2-3 ml
Children (>2 years): 3-5 ml
Older Children & Adults: 5-10 ml
Refrigerate until time of shipment. Ship sample within 5 days of collection at room temperature with overnight delivery.
Muscle Biopsy1-2 mm in length or > 100 mg is acceptable.

Flash freeze sample upon collection using liquid nitrogen. If storage is required, store sample at -80o C or colder.
Ship frozen sample on dry ice with overnight delivery.
CPT Codes 81401 (x1)

cap certification
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