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Results 1 - 10 of 173 for Abnormality of movement
  1. TUBB4A gene 
    ... breakdown (atrophy) of brain tissue in these regions, movement abnormalities, difficulty swallowing and speaking, and learning problems.The ... particularly in the putamen, cerebellum, and white matter. Abnormalities in ... underlie the movement, speech, and learning problems that can occur in ...
    https://medlineplus.gov/genetics/gene/tubb4a - Genetics
  2. PLA2G6 gene 
    ... also caused by PLA2G6 gene mutations and involves movement abnormalities that occur in adulthood. Dystonia is involuntary tensing of the muscles, and parkinsonism comprises a group of movement problems including unusually slow movement (bradykinesia), muscle rigidity, ...
    https://medlineplus.gov/genetics/gene/pla2g6 - Genetics
  3. SLC6A3 gene 
    ... unclear how altered dopamine signaling causes the specific movement abnormalities found in people with dopamine transporter deficiency syndrome.Studies suggest that the age at which signs and symptoms appear is related ... develop movement problems starting in infancy most often have transporter ...
    https://medlineplus.gov/genetics/gene/slc6a3 - Genetics
  4. MECP2 gene 
    ... intellectual disability, bipolar disorder, and a pattern of movement abnormalities known as parkinsonism. This condition affects males more ...
    https://medlineplus.gov/genetics/gene/mecp2 - Genetics
  5. ABCB7 gene 
    ... problems with coordination and balance (ataxia) and other movement abnormalities. More About This Health Condition ABC transporter 7 ...
    https://medlineplus.gov/genetics/gene/abcb7 - Genetics
  6. CLPB gene 
    ... This condition is characterized by neurological problems, including movement abnormalities and seizures; a shortage of white blood cells ( ...
    https://medlineplus.gov/genetics/gene/clpb - Genetics
  7. NKX2-1 gene 
    ... interneuron formation or migration, which may underlie the movement abnormalities characteristic of brain-lung-thyroid syndrome. More About ...
    https://medlineplus.gov/genetics/gene/nkx2-1 - Genetics
  8. SPR gene 
    ... brain. The shortage of these neurotransmitters causes the movement abnormalities and other features of sepiapterin reductase deficiency.Sepiapterin ...
    https://medlineplus.gov/genetics/gene/spr - Genetics
  9. EPM2A gene 
    ... The degeneration of neurons likely underlies the seizures, movement abnormalities, intellectual decline, and other neurological problems seen with ...
    https://medlineplus.gov/genetics/gene/epm2a - Genetics
  10. DCTN1 gene 
    ... brain disease is characterized by a pattern of movement abnormalities known as parkinsonism, psychiatric changes, weight loss, and ...
    https://medlineplus.gov/genetics/gene/dctn1 - Genetics
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