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Results 11 - 20 of 38 for Dystonia 30
  1. Early-onset isolated dystonia 
    ... never know they have the altered gene. Only 30 to 40 percent of people who inherit a TOR1A gene variant will ever develop signs and symptoms of early-onset isolated dystonia.The vast majority of those who have been ...
    https://medlineplus.gov/.../condition/early-onset-isolated-dystonia - Genetics
  2. SUCLA2-related mitochondrial DNA depletion syndrome 
    ... related mtDNA depletion syndrome can include uncontrolled movements (dystonia), hearing ... 30 percent of individuals with SUCLA2-related mtDNA depletion ...
    https://medlineplus.gov/...ated-mitochondrial-dna-depletion-syndrome - Genetics
  3. Task-specific focal dystonia 
    ... Embouchure dystonia--Portrait of a task-specific cranial dystonia. Mov Disord. ... disorders in musicians. Mov Disord. 2008 Oct 30;23(14):1957-65. doi: 10.1002/mds. ...
    https://medlineplus.gov/.../condition/task-specific-focal-dystonia - Genetics
  4. TUBB4A gene 
    ... autoregulatory domain of beta-tubulin 4a cause hereditary dystonia. Ann Neurol. 2013 ... paraplegia. Mov Disord. 2015 May;30(6):854-8. doi: 10.1002/mds.26196. ...
    https://medlineplus.gov/genetics/gene/tubb4a - Genetics
  5. Sepiapterin reductase deficiency 
    ... pattern of involuntary, sustained muscle contractions known as dystonia. Other movement problems can include muscle stiffness (spasticity), ... signs and symptoms of the condition. Dopa-responsive dystonia due to sepiapterin reductase deficiency SPR deficiency Genetic ...
    https://medlineplus.gov/.../sepiapterin-reductase-deficiency - Genetics
  6. Familial paroxysmal kinesigenic dyskinesia 
    ... An episode may involve slow, prolonged muscle contractions (dystonia); small, fast, "dance-like" motions (chorea); writhing movements ... affected person has one parent with the condition. Dystonia 10 Episodic kinesigenic dyskinesia Familial paroxysmal dystonia Paroxysmal ...
    https://medlineplus.gov/...amilial-paroxysmal-kinesigenic-dyskinesia - Genetics
  7. Autosomal dominant sleep-related hypermotor epilepsy 
    ... that can be effectively managed with medication, approximately 30 percent of affected individuals have seizures that become ... Clin Transl Neurol. 2015 Aug;2(8):821-30. doi: 10.1002/acn3.224. Epub 2015 Jul ...
    https://medlineplus.gov/...ominant-sleep-related-hypermotor-epilepsy - Genetics
  8. Beta-propeller protein-associated neurodegeneration 
    ... dementia). Worsening problems with movement also occur, including dystonia and parkinsonism. Dystonia is a condition characterized by involuntary, sustained muscle ...
    https://medlineplus.gov/...ller-protein-associated-neurodegeneration - Genetics
  9. GLUT1 deficiency syndrome 
    ... as ataxia or involuntary tensing of various muscles (dystonia); the movement problems may be more pronounced than ... deficiency syndrome. These include paroxysmal choreoathetosis with spasticity (dystonia 9); paroxysmal exercise-induced dyskinesia and epilepsy (dystonia ...
    https://medlineplus.gov/genetics/condition/glut1-deficiency-syndrome - Genetics
  10. TUBB4A-related leukodystrophy 
    ... other movement abnormalities, such as involuntary muscle contractions (dystonia), uncontrolled movements of the limbs (choreoathetosis), muscle stiffness ( ...
    https://medlineplus.gov/.../condition/tubb4a-related-leukodystrophy - Genetics
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