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Results 1 - 10 of 26 for dystonia
  1. TOR1A gene 
    ... gene causes most cases of early-onset isolated dystonia. This condition is one of many forms of dystonia, which is a group of conditions characterized by ...
    https://medlineplus.gov/genetics/gene/tor1a - Genetics
  2. GCH1 gene 
    ... gene have been found to cause dopa-responsive dystonia. This condition is characterized by a pattern of involuntary muscle contractions (dystonia), tremors, and other uncontrolled movements and usually responds ...
    https://medlineplus.gov/genetics/gene/gch1 - Genetics
  3. TUBB4A gene 
    ... been found to cause another neurological disorder called dystonia 4 (also known as DYT4 dystonia or whispering dysphonia), which is characterized by a ...
    https://medlineplus.gov/genetics/gene/tubb4a - Genetics
  4. THAP1 gene 
    ... gene mutations have been identified in people with dystonia 6. Dystonia 6 is one of many forms of dystonia, which is a group of conditions characterized by ...
    https://medlineplus.gov/genetics/gene/thap1 - Genetics
  5. SPR gene 
    ... gene have been found to cause dopa-responsive dystonia. This condition is characterized by a pattern of involuntary muscle contractions (dystonia), tremors, and other uncontrolled movements and usually responds ...
    https://medlineplus.gov/genetics/gene/spr - Genetics
  6. SGCE gene 
    ... SGCE gene have been found to cause myoclonus-dystonia, which is a movement disorder characterized by involuntary ... leads to the involuntary movements characteristic of myoclonus-dystonia. It is unknown why SGCE gene mutations seem ...
    https://medlineplus.gov/genetics/gene/sgce - Genetics
  7. PRKRA gene 
    ... PRKRA gene have been identified in people with dystonia 16. This condition is one of many forms of dystonia, which is a group of conditions characterized by ...
    https://medlineplus.gov/genetics/gene/prkra - Genetics
  8. TH gene 
    ... found to cause a form of dopa-responsive dystonia called TH-deficient dopa-responsive dystonia. This condition is characterized by a pattern of involuntary muscle contractions (dystonia), tremors, and other uncontrolled movements. These symptoms usually ...
    https://medlineplus.gov/genetics/gene/th - Genetics
  9. TIMM8A gene 
    ... TIMM8A gene have been found to cause deafness-dystonia-optic neuronopathy (DDON) syndrome. Most of these mutations ... More About This Health Condition DDP DDP1 deafness/dystonia peptide DFN1 MGC12262 TIM8A_HUMAN translocase of inner ...
    https://medlineplus.gov/genetics/gene/timm8a - Genetics
  10. SLC30A10 gene 
    ... have been identified in people with hypermanganesemia with dystonia, polycythemia, and cirrhosis (HMDPC, also known as hypermanganesemia with dystonia 1). This inherited disorder is characterized by high ...
    https://medlineplus.gov/genetics/gene/slc30a10 - Genetics
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