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Results 21 - 30 of 35 for Orofacial dyskinesia
  1. Leber hereditary optic neuropathy 
    ... loss, the features of LHON plus can include movement disorders, tremors, and abnormalities of the electrical signals that ...
    https://medlineplus.gov/.../leber-hereditary-optic-neuropathy - Genetics
  2. CLPB deficiency 
    ... progressive brain atrophy, intellectual disability, congenital neutropenia, cataracts, movement disorder. Am J Hum Genet. 2015 Feb 5;96( ...
    https://medlineplus.gov/genetics/condition/clpb-deficiency - Genetics
  3. Dopa-responsive dystonia 
    ... in people who have symptoms similar to other movement disorders. Mutations in the GCH1 gene are the most ...
    https://medlineplus.gov/genetics/condition/dopa-responsive-dystonia - Genetics
  4. Tetrahydrobiopterin deficiency 
    ... can include intellectual disability, progressive problems with development, movement disorders, difficulty swallowing, seizures, behavioral problems, and an inability ...
    https://medlineplus.gov/.../condition/tetrahydrobiopterin-deficiency - Genetics
  5. Autosomal recessive congenital methemoglobinemia 
    ... these cells likely contributes to the encephalopathy and movement disorders characteristic of autosomal recessive congenital methemoglobinemia type II. ...
    https://medlineplus.gov/...al-recessive-congenital-methemoglobinemia - Genetics
  6. Benign essential blepharospasm 
    ... type of dystonia, which is a group of movement disorders that involve uncontrolled tensing of the muscles (muscle ...
    https://medlineplus.gov/.../condition/benign-essential-blepharospasm - Genetics
  7. Mucopolysaccharidosis type III 
    ... III may develop seizures, loss of mobility, and movement disorders.The physical features of MPS III are less ...
    https://medlineplus.gov/.../condition/mucopolysaccharidosis-type-iii - Genetics
  8. Wiedemann-Rautenstrauch syndrome 
    ... Spectrum of Pediatric to Early Adulthood POLR3A-Associated Movement Disorders. Mov Disord Clin Pract. 2022 Dec 23;10( ...
    https://medlineplus.gov/.../wiedemann-rautenstrauch-syndrome - Genetics
  9. Pearson syndrome 
    ... eyelids (ptosis), vision problems, hearing loss, seizures, or movement disorders. About half of children with this severe disorder ...
    https://medlineplus.gov/genetics/condition/pearson-syndrome - Genetics
  10. CLN1 disease 
    ... adulthood. Adults with CLN1 disease may also have movement disorders, including impaired muscle coordination (ataxia) or a pattern ...
    https://medlineplus.gov/genetics/condition/cln1-disease - Genetics
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