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Results 31 - 40 of 69 for Dystonia 9
  1. 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
  2. DRD5 gene 
    ... PubMed Misbahuddin A, Placzek MR, Warner TT. Focal dystonia is associated with a polymorphism of the dopamine ... T, Bandmann O. Candidate gene studies in focal dystonia. Neurology. 2003 Oct 28;61(8):1097-101. ...
    https://medlineplus.gov/genetics/gene/drd5 - Genetics
  3. Biotin-thiamine-responsive basal ganglia disease 
    ... and can include involuntary tensing of various muscles (dystonia), muscle rigidity, muscle weakness on one or both ... individuals, the neurological problems are usually limited to dystonia, seizure disorders, and delay in the development of ...
    https://medlineplus.gov/...thiamine-responsive-basal-ganglia-disease - Genetics
  4. ADCY5-related dyskinesia 
    ... as sudden (paroxysmal) jerks, twitches, tremors, muscle tensing (dystonia), or writhing (choreiform) movements, and can affect the ... mutation causes early-onset autosomal dominant chorea and dystonia. Mov Disord. 2015 Mar;30(3):423-7. ...
    https://medlineplus.gov/genetics/condition/adcy5-related-dyskinesia - Genetics
  5. Ataxia with oculomotor apraxia 
    ... oculomotor apraxia, individuals with this type typically develop dystonia, which is involuntary, sustained muscle tensing that causes unusual positioning of body parts. Dystonia can be the first feature of the condition, ...
    https://medlineplus.gov/.../condition/ataxia-with-oculomotor-apraxia - Genetics
  6. MT-ND6 gene 
    ... hereditary optic neuropathy and a movement disorder called dystonia, which involves involuntary muscle contractions, tremors, and other ... of Leigh syndrome, Leber hereditary optic neuropathy, or dystonia. It also remains unclear why a single variant ...
    https://medlineplus.gov/genetics/gene/mt-nd6 - Genetics
  7. SUCLA2 gene 
    ... associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness. Brain. 2007 Mar;130(Pt 3): ... 243-52. doi: 10.1007/s10545-015-9894-9. Epub 2015 Oct 16. Citation on PubMed Chinnery ...
    https://medlineplus.gov/genetics/gene/sucla2 - Genetics
  8. Pontocerebellar hypoplasia 
    ... abnormal patterns of movement described as chorea or dystonia, and stiffness (spasticity). Many also have impaired vision ... PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10 PONTOCEREBELLAR HYPOPLASIA, TYPE 9; PCH9 PONTOCEREBELLAR HYPOPLASIA, TYPE 8; PCH8 PONTOCEREBELLAR HYPOPLASIA, ...
    https://medlineplus.gov/.../condition/pontocerebellar-hypoplasia - Genetics
  9. CHMP2B-related frontotemporal dementia 
    ... movement abnormalities include rigidity, tremors, uncontrolled muscle tensing (dystonia), and involuntary muscle spasms (myoclonus). As the disease ... chromosome 3. Hum Mol Genet. 1995 Sep;4(9):1625-8. doi: 10.1093/hmg/4.9. ...
    https://medlineplus.gov/.../chmp2b-related-frontotemporal-dementia - Genetics
  10. Pyridoxine-dependent epilepsy 
    ... include low body temperature (hypothermia), poor muscle tone (dystonia) soon after birth, and irritability before a seizure ... Arch Dis Child. 2007 Aug;92(8):687-9. doi: 10.1136/adc.2006.103192. Epub 2006 ...
    https://medlineplus.gov/.../condition/pyridoxine-dependent-epilepsy - Genetics
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