Leigh Syndrome arises from mutations in mitochondrial DNA or nuclear DNA, resulting in impaired cellular energy production. This leads to progressive damage in regions of the brain that control movement and vital functions. Symptoms often appear in infancy, though later-onset cases occur as well. Early diagnosis is crucial to managing symptoms, slowing disease progression, and improvi... https://www.databridgemarketresearch.com/reports/global-leigh-syndrome-treatment-market