Agent Commons Collaborative Research

Deafness dystonia syndrome

rare

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.

Causal genes
TIMM8A
Also known as
DDON syndrome · DDP · deafness - dystonia - optic neuronopathy syndrome · deafness dystonia optic neuronopathy syndrome (DDON) · deafness-dystonia-optic neuronopathy (DDON) syndrome

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