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Results 1 - 9 of 9 for "Dystonia," "adult-onset"
  1. MT-ND1 gene 
    ... has been reported in a few cases of adult-onset dystonia. Dystonia is a movement disorder that involves involuntary ... environmental factors to increase the risk of developing adult-onset dystonia. mitochondrially encoded NADH dehydrogenase 1 MTND1 NADH dehydrogenase ...
    https://medlineplus.gov/genetics/gene/mt-nd1 - Genetics
  2. TOR1A gene 
    ... in the TOR1A gene and several forms of adult-onset dystonia. One of these forms of dystonia, benign essential ... are related to benign essential blepharospasm and other adult-onset dystonias. More About This Health Condition Dystonia 1 protein DYT1 TOR1A_HUMAN Torsin-1A torsinA ...
    https://medlineplus.gov/genetics/gene/tor1a - Genetics
  3. Benign essential blepharospasm 
    ... condition may be related to other forms of adult-onset dystonia, including uncontrolled twisting of the neck muscles (spasmodic ... history of this disorder or other forms of dystonia in their family. Less commonly, benign essential blepharospasm has ... G, Berardelli A, Hallett M. Do primary adult-onset focal dystonias share aetiological factors? Brain. 2007 May; ...
    https://medlineplus.gov/.../condition/benign-essential-blepharospasm - Genetics
  4. Dopa-responsive dystonia 
    ... Rarely, the movement problems associated with dopa-responsive dystonia do not appear until adulthood. In these adult-onset cases, parkinsonism usually develops before dystonia, and movement ...
    https://medlineplus.gov/genetics/condition/dopa-responsive-dystonia - Genetics
  5. Hypermanganesemia with dystonia 
    ... between ages 2 and 15, or in adulthood (adult-onset). Most children with the early-onset form of HMDPC experience dystonia in the arms and legs, which often leads ...
    https://medlineplus.gov/.../hypermanganesemia-with-dystonia - Genetics
  6. Neuroferritinopathy 
    ... coordinating movements (ataxia), or uncontrolled tensing of muscles (dystonia). Symptoms of ... Ferritin-related neurodegeneration Hereditary ferritinopathy NBIA3 Neurodegeneration with ...
    https://medlineplus.gov/genetics/condition/neuroferritinopathy - Genetics
  7. Ataxia with oculomotor apraxia 
    ... tensing that causes unusual positioning of body parts. Dystonia can be the first feature of ... Adult onset ataxia with oculomotor apraxia EAOH Early-onset ataxia ...
    https://medlineplus.gov/.../condition/ataxia-with-oculomotor-apraxia - Genetics
  8. Mitochondrial membrane protein-associated neurodegeneration 
    ... including muscle stiffness (spasticity) and involuntary muscle cramping (dystonia). Many people with MPAN ... in adult-onset mitochondrial membrane protein-associated neurodegeneration. Clin Genet. 2013 ...
    https://medlineplus.gov/...rane-protein-associated-neurodegeneration - Genetics
  9. 3-methylglutaconyl-CoA hydratase deficiency 
    ... skills (psychomotor delay), speech delay, involuntary muscle cramping (dystonia), and spasms and ... type I causes leukoencephalopathy of adult onset. Neurology. 2006 Nov 28;67(10):1895-6. ...
    https://medlineplus.gov/...methylglutaconyl-coa-hydratase-deficiency - Genetics