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Results 1 - 10 of 18 for Tardive dyskinesia
  1. RAD51 gene 
    ... have been identified in people with congenital mirror movement disorder, a condition in which intentional movements of one ... in the signs and symptoms of congenital mirror movement disorder. More About This Health Condition MedlinePlus Genetics provides ...
    https://medlineplus.gov/genetics/gene/rad51 - Genetics
  2. DCC gene 
    ... have been identified in people with congenital mirror movement disorder, a condition in which intentional movements of one ...
    https://medlineplus.gov/genetics/gene/dcc - Genetics
  3. DLG4 gene 
    ... development and often causes intellectual disabilies, delayed development, movement disorders, and seizures. Most of the variants impair the ...
    https://medlineplus.gov/genetics/gene/dlg4 - Genetics
  4. TRPM6 gene 
    ... of motor neurons, leading to neurological problems and movement disorders characteristic of this condition. If the condition is ...
    https://medlineplus.gov/genetics/gene/trpm6 - Genetics
  5. HEXA gene 
    ... disease is a condition that is characterized by movement disorders, intellectual and developmental disability, and other neurological problems ...
    https://medlineplus.gov/genetics/gene/hexa - Genetics
  6. AUH gene 
    ... deficiency. This condition causes neurological problems such as movement disorders and problems with thinking ability (cognition). The mutations ...
    https://medlineplus.gov/genetics/gene/auh - Genetics
  7. MT-ND1 gene 
    ... cases of adult-onset dystonia. Dystonia is a movement disorder that involves involuntary tensing of the muscles (muscle ...
    https://medlineplus.gov/genetics/gene/mt-nd1 - Genetics
  8. MT-ND6 gene 
    ... people with Leber hereditary optic neuropathy and a movement disorder called dystonia, which involves involuntary muscle contractions, tremors, ...
    https://medlineplus.gov/genetics/gene/mt-nd6 - Genetics
  9. MECP2 gene 
    ... and is characterized by small head size (microcephaly), movement disorders, breathing problems, and seizures. Many of the MECP2 ...
    https://medlineplus.gov/genetics/gene/mecp2 - Genetics
  10. CYB5R3 gene 
    ... these cells likely contributes to the encephalopathy and movement disorders characteristic of autosomal recessive congenital methemoglobinemia type II. ...
    https://medlineplus.gov/genetics/gene/cyb5r3 - Genetics
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