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Results 1 - 10 of 16 for abnormal involuntary movement
  1. ADCY5 gene 
    ... with ADCY5-related dyskinesia, a disorder that causes abnormal involuntary movements. These mutations are thought to enhance adenylate cyclase 5 enzyme activity and lead to higher levels of cAMP within cells, so they ... leads to the abnormal movements that occur in this disorder. More About ...
    https://medlineplus.gov/genetics/gene/adcy5 - Genetics
  2. FRMD7 gene 
    ... areas of the brain that control eye movement. Abnormal development of these nerve cells likely causes the involuntary side-to-side eye movements that are characteristic of X-linked infantile nystagmus. ...
    https://medlineplus.gov/genetics/gene/frmd7 - Genetics
  3. LMNB1 gene 
    ... thirties or forties. The autonomic nervous system controls involuntary body ... result from an abnormal extra copy (duplication) of the LMNB1 gene. As ...
    https://medlineplus.gov/genetics/gene/lmnb1 - Genetics
  4. CASK gene 
    ... with or without nystagmus. Nystagmus refers to rapid, involuntary back-and-forth ... More About This Health Condition MedlinePlus ...
    https://medlineplus.gov/genetics/gene/cask - Genetics
  5. PRKRA gene 
    ... which is a group of conditions characterized by involuntary movements, ... to stress. The abnormal signaling increases the rate at which cell death ...
    https://medlineplus.gov/genetics/gene/prkra - Genetics
  6. GCH1 gene 
    ... This condition is characterized by a pattern of involuntary muscle ... believe that the abnormal enzyme may interfere with the activity of the ...
    https://medlineplus.gov/genetics/gene/gch1 - Genetics
  7. SNCA gene 
    ... controlling the start and stop of voluntary and involuntary movements. Alpha-synuclein may also play a role in ... of this condition is Lewy bodies, which are abnormal clusters of alpha-synuclein protein in the brain. ...
    https://medlineplus.gov/genetics/gene/snca - Genetics
  8. PRRT2 gene 
    ... those that occur in BFIS and episodes of involuntary movements like those that occur in familial paroxysmal kinesigenic ...
    https://medlineplus.gov/genetics/gene/prrt2 - Genetics
  9. CACNA1F gene 
    ... light (photophobia), a loss of sharpness (reduced acuity), involuntary movements of the eyes (nystagmus). Many affected individuals also ... front part of the eye (astigmatism), nearsightedness (myopia), abnormal color vision, and night blindness. The variant associated ...
    https://medlineplus.gov/genetics/gene/cacna1f - Genetics
  10. CACNA1A gene 
    ... episodes of poor coordination and balance (ataxia) and involuntary eye movements called nystagmus. The CACNA1A variants that cause EA2 ... usual, which increases the release of neurotransmitters. The abnormal signaling between neurons caused by these changes leads ...
    https://medlineplus.gov/genetics/gene/cacna1a - Genetics
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