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Results 11 - 20 of 34 for Dystonia 25
  1. 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
  2. MT-ND1 gene 
    ... reported in a few cases of adult-onset dystonia. Dystonia is a movement disorder that involves involuntary tensing ... 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
  3. 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
  4. McLeod neuroacanthocytosis syndrome 
    ... of the arms and legs, and muscle tensing (dystonia) in the face and throat, which can cause ... vocal tics (such as grunting and clicking noises). Dystonia of the tongue can lead to swallowing difficulties. ...
    https://medlineplus.gov/.../mcleod-neuroacanthocytosis-syndrome - Genetics
  5. 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
  6. 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
  7. 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
  8. Leigh syndrome 
    ... develop weak muscle tone (hypotonia), involuntary muscle contractions (dystonia), and problems with movement and balance (ataxia). Loss ... third of cases of the condition. At least 25 genes involved in the formation of complex I, ...
    https://medlineplus.gov/genetics/condition/leigh-syndrome - Genetics
  9. Baraitser-Winter syndrome 
    ... with Baraitser-Winter syndrome have involuntary muscle tensing (dystonia). Baraitser-Winter syndrome is a rare condition. Fewer ... a new syndrome. J Med Genet. 1988 Jan;25(1):41-3. doi: 10.1136/jmg.25. ...
    https://medlineplus.gov/genetics/condition/baraitser-winter-syndrome - Genetics
  10. Deep Brain Stimulation (DBS) for the Treatment of Parkinson's Disease and other Movement Disorders From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Movement Disorders/Statistics and Research ... Movement Disorders ... Parkinson's Disease/Statistics and Research ... Parkinson's Disease ... National Institute of Neurological ...
    https://www.ninds.nih.gov/...ns-disease-and-other-movement-disorders - External Health Links
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