Odone Syndrome is a rare genetic disorder that primarily affects the nervous system. It is characterized by progressive loss of motor skills, cognitive decline, and behavioral changes. The syndrome is often associated with mutations in the ABCD1 gene, which plays a crucial role in the metabolism of fatty acids in the brain. Symptoms typically appear in early childhood and can include difficulty walking, speech problems, and seizures. As the condition progresses, individuals may experience severe disabilities. Early diagnosis and supportive care are essential for managing symptoms and improving quality of life for those affected by Odone Syndrome.