Progressive exterior ophthalmoplegia

 Progressive exterior ophthalmoplegia - mitochondrion disturbance. It is characterized plural mitohondrialnym by DNA deleting in a sceletal muscle. The most blanket clinical signs include the adult beginning of delicacy of exterior eye muscles (ophthalmoplegia) and lack of tolerance of realization.  Additional symptoms are variables, and can include cataracts, hearing losses, a sensory axonal neuropathy, ataksiju, dropping, hypogonadism, both a parkinsonism. And the autosomal majorant and autosomal recessive inheritance can meet; autosomal recessive inheritance is usually more serious.

 It is usually diagnosed nevrpatologami. There is no proved treatment; the observational agents such as "coenyzme Q10" can provide advantage.