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Results 21 - 30 of 69 for Dystonia 9
  1. SPR gene 
    ... 1007/s10545-009-1067-2. Epub 2009 Feb 9. Erratum In: J Inherit Metab Dis. 2009 ... with dopa-responsive dystonia. Neurogenetics. 2004 Sep;5(3):187-90. doi: ...
    https://medlineplus.gov/genetics/gene/spr - Genetics
  2. Pantothenate kinase-associated neurodegeneration 
    ... syndrome. Nat Genet. 2001 Aug;28(4):345-9. doi: 10.1038/ng572. Citation on PubMed
    https://medlineplus.gov/...enate-kinase-associated-neurodegeneration - Genetics
  3. MT-ND1 gene 
    ... J Med Genet. 2006 Feb;43(2):175-9. doi: 10.1136/jmg.2005.032474. Epub 2005 Jun ... mutation in adult-onset dystonia. Neurogenetics. 2003 Aug;4(4):199-205. doi: ...
    https://medlineplus.gov/genetics/gene/mt-nd1 - Genetics
  4. Primary coenzyme Q10 deficiency 
    ... disability, poor muscle tone (hypotonia), involuntary muscle contractions (dystonia), progressive muscle stiffness (spasticity), abnormal eye movements (nystagmus), ...
    https://medlineplus.gov/.../primary-coenzyme-q10-deficiency - Genetics
  5. ATP1A3 gene 
    ... gene-identification study. Lancet Neurol. 2012 Sep;11(9):764-73. doi: ... case of rapid-onset dystonia-parkinsonism. J Neurol Sci. 2008 Oct 15;273( ...
    https://medlineplus.gov/genetics/gene/atp1a3 - 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. ARX gene 
    ... and a group of movement problems called focal dystonia that primarily affects the hands. The most common ... developing brain, leading to the intellectual disability and dystonia characteristic of Partington syndrome. More About This Health ...
    https://medlineplus.gov/genetics/gene/arx - 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. MEGDEL syndrome 
    ... with MEGDEL syndrome later develop involuntary muscle tensing (dystonia) and muscle stiffness (spasticity), which worsen over time. ... mitochondrial function and intracellular cholesterol trafficking and cause dystonia and deafness. Nat Genet. 2012 Jun 10;44( ...
    https://medlineplus.gov/genetics/condition/megdel-syndrome - Genetics
  10. SUCLA2-related mitochondrial DNA depletion syndrome 
    ... related mtDNA depletion syndrome can include uncontrolled movements (dystonia), hearing loss, muscle wasting (atrophy), and intellectual disabilities. ... associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness. Brain. 2007 Mar;130(Pt 3): ...
    https://medlineplus.gov/...ated-mitochondrial-dna-depletion-syndrome - Genetics
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