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Results 1 - 10 of 17 for Multiple system atrophy
  1. Multiple system atrophy 
    Multiple system atrophy is a progressive brain disorder that affects movement and balance and disrupts the function of the autonomic nervous system. The autonomic ...
    https://medlineplus.gov/genetics/condition/multiple-system-atrophy - Genetics
  2. COQ2 gene 
    ... have been suggested to increase the risk of multiple system atrophy, a progressive brain disorder that affects movement and ... are associated with an increased risk of developing multiple system atrophy in the Japanese population. However, studies have not ...
    https://medlineplus.gov/genetics/gene/coq2 - Genetics
  3. SNCA gene 
    ... have been found to increase the risk of multiple system atrophy, a progressive brain disorder that affects movement and ... and how they influence the risk of developing multiple system atrophy. Variations in the SNCA gene appear to affect ...
    https://medlineplus.gov/genetics/gene/snca - Genetics
  4. Orthostatic hypotension 
    ... as Parkinson's disease, dementia with Lewy bodies, multiple system atrophy, pure autonomic failure, diabetes, Guillain-Barré syndrome, dopamine ...
    https://medlineplus.gov/genetics/condition/orthostatic-hypotension - Genetics
  5. Farber lipogranulomatosis 
    ... to the classic signs, Farber lipogranulomatosis often affects multiple body ... (hydrocephalus), loss (atrophy) of brain tissue, paralysis of the arms and ...
    https://medlineplus.gov/genetics/condition/farber-lipogranulomatosis - Genetics
  6. Dilated cardiomyopathy with ataxia syndrome 
    ... heart problems, movement difficulties, and other features affecting multiple body systems.Beginning in infancy to early childhood, most people ...
    https://medlineplus.gov/...lated-cardiomyopathy-with-ataxia-syndrome - Genetics
  7. FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome 
    ... severe condition that begins in infancy and affects multiple body systems. It is primarily associated with brain dysfunction combined ...
    https://medlineplus.gov/...thic-mitochondrial-dna-depletion-syndrome - Genetics
  8. Autosomal dominant cerebellar ataxia, deafness, and narcolepsy 
    ... methylation is abnormal, which affects the expression of multiple genes. Maintenance of the neurons that make up the nervous system is disrupted, leading to the signs and symptoms ...
    https://medlineplus.gov/...cerebellar-ataxia-deafness-and-narcolepsy - Genetics
  9. OPA1 gene 
    ... likely caused by the loss of cells in multiple tissues due to poor mitochondrial function. It is unclear why OPA1 gene mutations affect only the eyes in individuals with optic atrophy type 1 but have more widespread effects in ...
    https://medlineplus.gov/genetics/gene/opa1 - Genetics
  10. Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart 
    ... deacetylase and is required for the function of multiple signaling centers during mouse embryogenesis. Development. 2004 Jan;131(1):3-14. doi: 10.1242/dev.00908. Epub 2003 Nov 26. Citation on PubMed
    https://medlineplus.gov/...thout-anomalies-of-the-brain-eye-or-heart - Genetics
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