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Results 11 - 20 of 37 for Dystonia 16
  1. Benign essential blepharospasm 
    ... the eyelids. This condition is a type of dystonia, which is a group of movement disorders that ... people with benign essential blepharospasm, the symptoms of dystonia spread beyond the eyes to affect other facial ...
    https://medlineplus.gov/.../condition/benign-essential-blepharospasm - Genetics
  2. ATP1A3 gene 
    ... deep brain stimulation. Neurology. 2008 Apr 15;70(16 Pt 2):1501-3. doi: ... dystonia parkinsonism, interfere with Na+ interaction by distinct mechanisms. ...
    https://medlineplus.gov/genetics/gene/atp1a3 - Genetics
  3. Autosomal dominant nocturnal frontal lobe epilepsy 
    ... Dominant Sleep-Related Hypermotor (Hyperkinetic) Epilepsy. 2002 May 16 [updated 2023 Mar 23]. In: Adam MP, Feldman ...
    https://medlineplus.gov/...-dominant-nocturnal-frontal-lobe-epilepsy - Genetics
  4. PLA2G6 gene 
    ... also cause atypical neuroaxonal dystrophy and PLA2G6-related dystonia-parkinsonism, which are conditions in which deterioration of ... not evident until the teenage years.PLA2G6-related dystonia-parkinsonism is also caused by PLA2G6 gene mutations ...
    https://medlineplus.gov/genetics/gene/pla2g6 - Genetics
  5. SLC39A14 gene 
    ... mutations have been found to cause hypermanganesemia with dystonia 2, a condition that begins in early childhood ... and brain (hypermanganesemia), involuntary tensing of the muscles (dystonia), and other movement problems. These mutations impair the ...
    https://medlineplus.gov/genetics/gene/slc39a14 - Genetics
  6. 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
  7. Aromatic l-amino acid decarboxylase deficiency 
    ... muscle contractions that may cause unusual body positions (dystonia) and writhing movements of the limbs (athetosis). Dystonia tends to become worse when the individual is ...
    https://medlineplus.gov/...tic-l-amino-acid-decarboxylase-deficiency - Genetics
  8. 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
  9. BTK gene 
    ... known as TIMM8A. Mutations in TIMM8A cause deafness-dystonia-optic neuronopathy (DDON) syndrome, which is characterized by ... in intellectual function (dementia), and involuntary muscle tensing (dystonia) or difficulty coordinating movements (ataxia). Individuals with large ...
    https://medlineplus.gov/genetics/gene/btk - Genetics
  10. Pelizaeus-Merzbacher disease 
    ... neck tremors (titubation), involuntary tensing of the muscles (dystonia), and jerking (choreiform) movements.Connatal Pelizaeus-Merzbacher disease ... j.jns.2004.10.010. Epub 2004 Dec 16. No abstract available. Citation on PubMed Inoue K. ...
    https://medlineplus.gov/.../condition/pelizaeus-merzbacher-disease - Genetics
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