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Results 21 - 30 of 31 for progressive cerebellar atrophy
  1. 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
  2. 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
  3. 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
  4. Degenerative Nerve Diseases (National Library of Medicine)  
    Degenerative nerve diseases affect many of your body's activities, such as balance, movement, talking, breathing, and heart function. Many of these diseases are genetic. ...
    https://medlineplus.gov/degenerativenervediseases.html - Health Topics
  5. 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
  6. 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
  7. 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
  8. 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
  9. Triosephosphate isomerase deficiency 
    ... of the brain involved in coordinating movements (the cerebellum) are particularly affected in people with triosephosphate isomerase ... T, Pissard S, Hachicha M. Hemolytic anemia and progressive neurologic impairment: think about triosephosphate isomerase deficiency. Fetal ...
    https://medlineplus.gov/.../triosephosphate-isomerase-deficiency - Genetics
  10. Brain and Spinal Cord Tumors From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Brain Tumors/Start Here ... Brain Tumors ... Spinal Cord Diseases/Start Here ... Spinal Cord Diseases ... Benign Tumors/Specifics ... Benign Tumors ... National Institute of Neurological ...
    https://www.ninds.nih.gov/.../disorders/brain-and-spinal-cord-tumors - External Health Links
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