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Results 1 - 7 of 7 for Oculomotor apraxia -Cogan type
Did you mean Oculomotor apraxia -organ type?
  1. Ataxia with oculomotor apraxia 
    ... s risk of developing heart disease.Ataxia with oculomotor apraxia type 2 usually begins around age 15. As in ... this type.A key feature of ataxia with oculomotor apraxia type 2 is high amounts of a protein called ...
    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 coordination ... cerebellum).PNKP gene mutations that cause ataxia with oculomotor apraxia type 4 lead to production of an unstable enzyme ...
    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 coordinating ... in senataxin. The mutations associated with ataxia with oculomotor apraxia type 2 are thought to disrupt the helicase function ...
    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 coordinating ... causing the characteristic movement problems of ataxia with oculomotor apraxia type 1. More About This Health Condition AOA AOA1 ...
    https://medlineplus.gov/genetics/gene/aptx - Genetics
  5. Cerebellar Disorders (National Library of Medicine)  
    When you play the piano or hit a tennis ball you are activating the cerebellum. The cerebellum is the area of the brain that controls coordination and balance. ...
    https://medlineplus.gov/cerebellardisorders.html - Health Topics
  6. 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
  7. TPP1 gene 
    ... and trouble moving the eyes side-to-side (oculomotor apraxia). People with SCAR7 have progressive loss of cells ( ... W, Miller N. Diagnosis of neuronal ceroid lipofuscinosis type 2 (CLN2 disease): Expert recommendations for early detection ...
    https://medlineplus.gov/genetics/gene/tpp1 - Genetics