Machado-Joseph disease, or MJD, also called spinocerebellar ataxia type 3, is a rare neurodegenerative disease inherited in an autosomal dominant pattern that causes progressive cerebellar ataxia, a loss of muscle control and coordination in the arms and legs. It results from an abnormal expansion of CAG trinucleotide repeats in the ATXN3 gene, which produces a faulty form of the protein ataxin and leads to the degeneration of cells in the hindbrain. Clumsiness and rigidity can lead it to be mistaken for drunkenness or Parkinson's disease. It is a type of spinocerebellar ataxia and the most common cause of dominantly inherited ataxia, producing paralysis of eye movement together with a mixed sensory and cerebellar ataxia. Its alternative names include Machado's disease, Joseph's disease and Machado-Joseph Azorean disease.
Facts
Classification
ICD-10 ChapterVI: Diseases of the Nervous System 1 Communicable or Non-communicable Causative Agent
Causative Agent (category) Prevalence Band Sources
1. Machado-Joseph disease (Wikipedia)
Lead section
rare autosomal dominantly inherited neurodegenerative disease
Lead section [causative-agent-category]
a genetic mutation that results in an expansion of abnormal "CAG" trinucleotide repeats in the ATXN3 gene
View the Source2. Orphadata (Orphanet): Orphadata epidemiology for ORPHA:98757 Spinocerebellar ataxia type 3
Orphadata (Orphanet)Prevalence, WorldwideQuote, Prevalence, Worldwide
"PrevalenceClass": "1-9 / 100 000", "PrevalenceGeographic": "Worldwide"
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