Leigh Syndrome Panel
Leigh Syndrome Panel
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Leigh syndrome is a serious neurological disorder that usually manifests itself in the first year of life. This condition is characterized by a progressive loss of mental and motor skills (psychomotor regression) and typically results in death within two to three years, usually due to respiratory failure.
The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.
- Available in less than 24 hours
- Based on Whole Genome Sequencing
- More than 35 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Leigh Syndrome

Dieses Produkt ist nur für Kunden gedacht, die bereits einen MyGenome-Test erworben haben.