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Results 1 - 10 of 21 for Progressive cerebellar ataxia
  1. Autosomal recessive cerebellar ataxia type 1 
    Autosomal recessive cerebellar ataxia 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 ...
    https://medlineplus.gov/...osomal-recessive-cerebellar-ataxia-type-1 - Genetics
  2. 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
  3. Autosomal dominant optic atrophy and cataract 
    ... can lead to problems with balance and coordination (cerebellar ataxia), an unsteady style of walking (gait), prickling or tingling sensations (paresthesias) in the arms and legs, progressive muscle stiffness (spasticity), or rhythmic shaking (tremors). In ...
    https://medlineplus.gov/...somal-dominant-optic-atrophy-and-cataract - Genetics
  4. Spinocerebellar ataxia type 6 
    ... the Ca(V)2.1 calcium channel in cerebellar ataxias. F1000 Biol Rep. 2010 Jan 18;2:4. doi: 10.3410/B2-4. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-6 - Genetics
  5. PRICKLE1-related progressive myoclonus epilepsy with ataxia 
    ... A, Leshinsky E, Berkovic SF. An autosomal recessive cerebellar ataxia syndrome with upward gaze palsy, neuropathy, and seizures. Neurology. 2005 Jan 11;64(1):142-4. doi: 10.1212/01.WNL.0000148600.60470.E6. Citation on PubMed
    https://medlineplus.gov/...rogressive-myoclonus-epilepsy-with-ataxia - Genetics
  6. Spinocerebellar ataxia type 3 
    ... magnetic resonance imaging features of the brainstem and cerebellum and clinical features of spinocerebellar ataxia 3/Machado-Joseph disease. Neurol India. 2009 Sep-Oct;57(5):578-83. doi: 10.4103/0028-3886.57803. Citation on PubMed
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-3 - Genetics
  7. Primary coenzyme Q10 deficiency 
    ... a person's sixties and often cause cerebellar ataxia, which refers to ... muscle stiffness (spasticity), abnormal eye movements (nystagmus), vision ...
    https://medlineplus.gov/.../primary-coenzyme-q10-deficiency - Genetics
  8. Mainzer-Saldino syndrome 
    ... of scar tissue in the liver (hepatic fibrosis); cerebellar ataxia, which is difficulty with coordination and balance arising ... Saldino disease MZSDS Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia, and skeletal dysplasia Saldino-Mainzer dysplasia Saldino-Mainzer ...
    https://medlineplus.gov/genetics/condition/mainzer-saldino-syndrome - Genetics
  9. Microcephaly, seizures, and developmental delay 
    ... van de Spek P, Kremer A, Mancini GM. Progressive cerebellar atrophy and polyneuropathy: expanding the spectrum of PNKP ...
    https://medlineplus.gov/...ocephaly-seizures-and-developmental-delay - Genetics
  10. Myoclonic epilepsy with ragged-red fibers 
    ... Kay CK, Raskin S, Werneck LC, Bruhn H. Cerebellar ataxia, myoclonus, cervical lipomas, and MERRF syndrome. Case report. ...
    https://medlineplus.gov/...myoclonic-epilepsy-with-ragged-red-fibers - Genetics
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