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Results 11 - 20 of 21 for progressive cerebellar atrophy
  1. Multiple system atrophy 
    Multiple system atrophy is a progressive brain disorder that affects movement and balance and disrupts the function of the autonomic nervous system. The autonomic ...
    https://medlineplus.gov/genetics/condition/multiple-system-atrophy - Genetics
  2. COQ2 gene 
    ... suggested to increase the risk of multiple system atrophy, a progressive brain disorder that affects movement and balance and ... H. Coenzyme Q10 Levels Are Decreased in the Cerebellum of Multiple-System Atrophy Patients. PLoS One. 2016 Feb 19;11(2): ...
    https://medlineplus.gov/genetics/gene/coq2 - Genetics
  3. Autosomal dominant cerebellar ataxia, deafness, and narcolepsy 
    ... P, Smith AM, Warman Chardon J. Autosomal dominant cerebellar ataxia, deafness, and narcolepsy (ADCA-DN) associated with progressive cognitive and behavioral deterioration. Neuropsychology. 2017 Mar;31( ...
    https://medlineplus.gov/...cerebellar-ataxia-deafness-and-narcolepsy - Genetics
  4. Spastic paraplegia type 15 
    ... over time. Additionally, there is often a loss (atrophy) of nerve cells in several parts of the brain, including the cerebral cortex, which controls thinking and emotions, and the cerebellum, which coordinates movement.People with this form of ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-15 - Genetics
  5. Charcot-Marie-Tooth disease 
    ... DISEASE, X-LINKED RECESSIVE, 4, WITH OR WITHOUT CEREBELLAR ATAXIA; CMTX4 ... OPTIC ATROPHY; HMSN6A NEUROPATHY, HEREDITARY MOTOR AND SENSORY, RUSSE TYPE; ...
    https://medlineplus.gov/.../condition/charcot-marie-tooth-disease - Genetics
  6. Spinocerebellar ataxia type 1 
    Spinocerebellar ataxia type 1 (SCA1) is a condition characterized by progressive problems with movement. People with this condition initially experience problems with ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-1 - Genetics
  7. Spinocerebellar ataxia type 2 
    ... type 2 (SCA2) is a condition characterized by progressive problems with movement. People with this condition initially ... Rub U, Auburger G. Spinocerebellar ataxia 2 (SCA2). Cerebellum. 2008;7(2):115-24. doi: 10.1007/ ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-2 - Genetics
  8. Myoclonic epilepsy with ragged-red fibers 
    ... characterized by muscle twitches (myoclonus), weakness (myopathy), and progressive stiffness (spasticity). When the muscle cells of affected ... Rufa A, Volpi N, Dotti MT, Federico A. Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with ...
    https://medlineplus.gov/...myoclonic-epilepsy-with-ragged-red-fibers - Genetics
  9. Leigh syndrome 
    ... year of life. This condition is characterized by progressive loss of mental and movement abilities (psychomotor regression) ... the basal ganglia, which help control movement; the cerebellum, which controls the ability to balance and coordinates ...
    https://medlineplus.gov/genetics/condition/leigh-syndrome - Genetics
  10. Walker-Warburg syndrome 
    ... of the brain, including a region called the cerebellum and the part of the brain that connects ... fibers weaken and die over time, leading to progressive weakness of the skeletal muscles.Defective α-dystroglycan ...
    https://medlineplus.gov/genetics/condition/walker-warburg-syndrome - Genetics
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