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Results 1 - 6 of 6 for Multiple system atrophy
  1. 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
  2. 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
  3. 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
  4. BICD2 gene 
    ... condition is characterized by muscle weakness and wasting (atrophy) in the ... in multiple affected individuals and families replaces the amino acid ...
    https://medlineplus.gov/genetics/gene/bicd2 - Genetics
  5. PMP22 gene 
    ... can result in loss of sensation and wasting (atrophy) of muscles in the feet, legs, and hands. ... brain. Typically beginning in adolescence, affected individuals experience atrophy of the muscles of the lower legs and ...
    https://medlineplus.gov/genetics/gene/pmp22 - Genetics
  6. ATP1A3 gene 
    ... of features: cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss. This specific presentation is ...
    https://medlineplus.gov/genetics/gene/atp1a3 - Genetics