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Deafness dystonia syndrome
rareAn 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.
- Identifiers
- MONDO:0010578 OMIM:304700Orphanet:52368
- 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
Projects
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