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Results 1 - 10 of 17 for progressive cerebellar atrophy
  1. Microcephaly, seizures, and developmental delay 
    ... van de Spek P, Kremer A, Mancini GM. Progressive cerebellar atrophy and polyneuropathy: expanding the spectrum of PNKP mutations. ...
    https://medlineplus.gov/...ocephaly-seizures-and-developmental-delay - Genetics
  2. Pontocerebellar hypoplasia 
    Pontocerebellar hypoplasia is a group of related conditions that affect the development of the brain. The term "pontocerebellar" refers to the pons and the cerebellum, ...
    https://medlineplus.gov/.../condition/pontocerebellar-hypoplasia - Genetics
  3. Autosomal recessive cerebellar ataxia type 1 
    ... type 1 (ARCA1) is a condition characterized by progressive problems with movement due to a loss (atrophy) of nerve cells in the part of the brain that coordinates movement (the cerebellum). Signs and symptoms of the disorder first appear ...
    https://medlineplus.gov/...osomal-recessive-cerebellar-ataxia-type-1 - Genetics
  4. Spinocerebellar ataxia type 36 
    ... SCA36.Brain imaging of people with SCA36 shows progressive atrophy of various parts of the brain, particularly within the cerebellum, which is the area of the brain involved ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-36 - Genetics
  5. Autosomal dominant optic atrophy and cataract 
    ... can lead to problems with balance and coordination (cerebellar ataxia), an unsteady ... Autosomal dominant optic atrophy and cataract is one form of autosomal dominant ...
    https://medlineplus.gov/...somal-dominant-optic-atrophy-and-cataract - Genetics
  6. Primary coenzyme Q10 deficiency 
    ... the brain that is involved in coordinating movement (cerebellum). Other ... caused by degeneration (atrophy) of the optic nerves or breakdown of the ...
    https://medlineplus.gov/.../primary-coenzyme-q10-deficiency - Genetics
  7. Pol III-related leukodystrophy 
    ... part of the brain involved in coordinating movements (cerebellar atrophy) and underdevelopment (hypoplasia) of tissue that connects the ... TACH); leukodystrophy with oligodontia (LO); or hypomyelination with cerebellar atrophy and hypoplasia of the corpus callosum (HCAHC). Because ...
    https://medlineplus.gov/.../condition/pol-iii-related-leukodystrophy - Genetics
  8. 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
  9. 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
  10. 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
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