Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy

Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy is a rare mitochondrial disease characterized by adult onset of progressive external ophthalmoplegia, exercise intolerance, muscle weakness, manifestations of spinocerebellar ataxia (e.g. impaired gait, dysarthria) and mild motor peripheral neuropathy. Respiratory insufficiency has been reported in some cases.

Also known as: adult-onset CPEO with mitochondrial myopathy

18 clinical trials for this condition and its sub-types, 0 tagged with Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy itself.