Leigh Syndrome Report

Leigh SyndromeLeigh syndrome is a rare genetic disorder that affects the central nervous system and can cause developmental delay, movement disorders, and respiratory failure. Leigh syndrome is caused by mutations in genes involved in mitochondrial function and energy production, and this report tests for genetic variants that are known to affect these processes.More than 20 genes analyzed It is recommended if: This report is designed for individuals with a family history of Leigh syndrome or individuals with symptoms of the condition, such as muscle weakness, poor coordination, and breathing problems. Genetic testing can confirm a diagnosis, provide information on disease severity and progression, and inform treatment and management decisions. Testing can also inform family planning decisions and provide reassurance for unaffected family members. List of main conditions: Leigh Syndrome