China Leigh Syndrome Treatment: An Informational Overview
Introduction
Leigh syndrome is a rare, inherited neurological disorder that typically begins in infancy or early childhood and affects the central nervous system. It is characterized by progressive degeneration of specific brain regions, especially those responsible for movement, breathing, and energy metabolism. In China, healthcare providers and researchers work to diagnose, manage, and support patients with this complex condition through multidisciplinary care.
What Leigh Syndrome Is
Leigh syndrome results from genetic mutations that impair mitochondrial function—the part of the cell responsible for producing energy. When mitochondria cannot generate sufficient energy, especially in high-demand tissues like the brain and muscles, cells can become damaged or die. This leads to a spectrum of neurological and systemic symptoms that can vary in severity and progression.