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Results 1 - 8 of 8 for Ataxia with oculomotor apraxia type 3
  1. Ataxia with oculomotor apraxia 
    ... or 4, respectively. Mutations in another gene cause ataxia with oculomotor apraxia type 3.The APTX, SETX, and PNKP genes provide instructions ... Ataxia - oculomotor apraxia type 4 Genetic Testing Registry: Ataxia with ... type 3 Genetic Testing Registry: Ataxia, early-onset, with oculomotor ...
    https://medlineplus.gov/.../condition/ataxia-with-oculomotor-apraxia - Genetics
  2. PNKP gene 
    ... P, Guerreiro R. Mutations in PNKP cause recessive ataxia with oculomotor apraxia type 4. Am J Hum Genet. 2015 Mar 5;96(3):474-9. doi: 10.1016/j.ajhg.2015. ...
    https://medlineplus.gov/genetics/gene/pnkp - Genetics
  3. SETX gene 
    ... B, Gueven N, Lavin MF. Senataxin, defective in ataxia oculomotor apraxia type 2, is involved in the defense against oxidative ...
    https://medlineplus.gov/genetics/gene/setx - Genetics
  4. APTX gene 
    ... the APTX gene have been found to cause ataxia with oculomotor apraxia type 1. This condition is characterized by difficulty coordinating ... the cerebellum, 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. Oculomotor Apraxia (American Association for Pediatric Ophthalmology and Strabismus)  
    Eye Movement Disorders/Specifics ... Eye Movement Disorders ... American Association for Pediatric Ophthalmology and Strabismus ... GLOSSARY, TERMS, ACRONYMS, PHRASES, ...
    https://www.aapos.org/glossary/oculomotor-apraxia - External Health Links
  7. Spinocerebellar ataxia type 36 
    Spinocerebellar ataxia type 36 (SCA36) is a condition characterized by progressive problems with movement that typically begin in mid-adulthood. ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-36 - Genetics
  8. TPP1 gene 
    ... gene have also been found to cause spinocerebellar ataxia, autosomal recessive ... (oculomotor apraxia). People with SCAR7 have progressive loss of cells ( ...
    https://medlineplus.gov/genetics/gene/tpp1 - Genetics