This product is only meant for customers who already
purchased a Sequencing Test
The Leigh Syndrome Report is based on Whole Genome Sequencing Test. As such, it analyzes all Common and Rare Variants associated with Leigh Syndrome, instead of a limited set of genes, like old genetic target panels.
Leigh Syndrome is a severe neurological disorder that usually becomes apparent in the first year of life. This condition is characterized by progressive loss of mental and movement abilities (psychomotor regression) and typically results in death within two to three years, usually due to respiratory failure.
Along with environmental factors, Genetics plays a key role in the regulation of Leigh Syndrome.
- 38 genes analyzed
- 100% genomic regions covered
- Intragenic and intergenic regions analyzed
- All variants reported
List of genes: