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Results 1 - 7 of 7 for Oculomotor apraxia
  1. Ataxia with oculomotor apraxia 
    Ataxia with oculomotor apraxia is a condition characterized by problems with movement that worsen over time. The hallmark of this condition is poor coordination ...
    https://medlineplus.gov/.../condition/ataxia-with-oculomotor-apraxia - Genetics
  2. PNKP gene 
    ... mutations have been found to cause ataxia with oculomotor apraxia type 4. This condition is characterized by poor ... with side-to-side movement of the eyes (oculomotor apraxia). These problems are due to the breakdown (degeneration) ...
    https://medlineplus.gov/genetics/gene/pnkp - Genetics
  3. SETX gene 
    ... gene have been found to cause ataxia with oculomotor apraxia type 2. This condition is characterized by difficulty ... with side-to-side movements of the eyes (oculomotor apraxia). Most mutations replace single protein building blocks (amino ...
    https://medlineplus.gov/genetics/gene/setx - Genetics
  4. APTX gene 
    ... gene have been found to cause ataxia with oculomotor apraxia type 1. This condition is characterized by difficulty ... with side-to-side movements of the eyes (oculomotor apraxia). Most mutations change single protein building blocks (amino ...
    https://medlineplus.gov/genetics/gene/aptx - Genetics
  5. Spinocerebellar ataxia type 36 
    ... saccades), trouble moving the eyes side-to-side (oculomotor apraxia), and droopy eyelids (ptosis). Sensorineural hearing loss, which ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-36 - Genetics
  6. Ataxia-telangiectasia 
    ... moving their eyes to look side-to-side (oculomotor apraxia). Small clusters of enlarged blood vessels called telangiectases, ...
    https://medlineplus.gov/genetics/condition/ataxia-telangiectasia - Genetics
  7. TPP1 gene 
    ... and trouble moving the eyes side-to-side (oculomotor apraxia). People with SCAR7 have progressive loss of cells ( ...
    https://medlineplus.gov/genetics/gene/tpp1 - Genetics