Deafness dystonia syndrome

An X-linked recessive neurodegenerative syndrome characterized by clinical manifestations commencing with early childhood onset hearing loss, followed by adolescent onset progressive dystonia or ataxia, visual impairment from early adulthood onwards and dementia from the 4th decade onwards.

Also known as: DDON syndrome, Deafness-Dystonia-Optic Neuronopathy Syndrome, Mohr-Tranebjaerg syndrome, Mohr-Tranebjaerg syndrome, X-linked recessive, deafness dystonia optic neuronopathy syndrome (DDON), deafness dystonia syndrome, deafness-dystonia-optic neuronopathy syndrome, DDP

0 clinical trials for this condition and its sub-types, 0 tagged with Deafness dystonia syndrome itself.