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Results 1 - 6 of 6 for "Sepiapterin%reductase%deficiency"
  1. Sepiapterin reductase deficiency 
    Sepiapterin reductase deficiency is a condition characterized by movement problems, most often a pattern of involuntary, sustained muscle contractions known as dystonia. ...
    https://medlineplus.gov/.../sepiapterin-reductase-deficiency - Genetics
  2. SPR gene 
    ... not occur in the brain. Therefore, people with sepiapterin reductase deficiency have a lack of tetrahydrobiopterin in the brain, ... the SPR gene have been found to cause sepiapterin reductase deficiency, a condition characterized by progressive problems with movement. ...
    https://medlineplus.gov/genetics/gene/spr - Genetics
  3. Dopa-responsive dystonia 
    ... Genetic Testing Registry: Dopa-responsive dystonia due to sepiapterin reductase deficiency Genetic Testing Registry: Dystonia 5 Genetic Testing Registry: ...
    https://medlineplus.gov/genetics/condition/dopa-responsive-dystonia - Genetics
  4. Dystonia (National Library of Medicine)  
    Dystonia is a movement disorder that causes involuntary contractions of your muscles. These contractions result in twisting and repetitive movements. Sometimes ...
    https://medlineplus.gov/dystonia.html - Health Topics
  5. Movement Disorders (National Library of Medicine)  
    Movement disorders are neurologic conditions that cause problems with movement, such as: Increased movement that can be voluntary (intentional) or involuntary ( ...
    https://medlineplus.gov/movementdisorders.html - Health Topics
  6. GCH1 gene 
    ... diagnosis and genetics of dopa-responsive dystonia and sepiapterin reductase deficiency. Mol Genet Metab. 2001 Sep-Oct;74(1- ...
    https://medlineplus.gov/genetics/gene/gch1 - Genetics