Type of neurodegenerative disorder with ataxia, dystonia, rigidity, and ophthalmoparesis; similar to spinocerebellar ataxia type 3. Defect is in MJd1 gene. Condition is autosomal dominant.
InsideSurgery Medical Information Blog
Details of surgical procedures, pathophysiology, signs and symptoms, and treatment of medical diseases,medical and surgical eponyms, and surgeons and surgery in the news