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Results 1 - 9 of 9 for spinocerebellar disease
  1. Spinocerebellar ataxia type 3 
    ... Joseph disease MJD SCA3 Genetic Testing Registry: Azorean disease Spinocerebellar ataxia type 3 National Organization for Rare Disorders ( ... the brainstem and cerebellum and clinical features of spinocerebellar ataxia 3/Machado-Joseph disease. Neurol India. 2009 Sep-Oct;57(5):578- ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-3 - Genetics
  2. Spinocerebellar ataxia type 1 
    ... HT. Pathogenic mechanisms of a polyglutamine-mediated neurodegenerative disease, spinocerebellar ataxia type 1. J Biol Chem. 2009 Mar ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-1 - Genetics
  3. Huntington's disease-like 
    ... Registry: Huntington disease-like 2 Genetic Testing Registry: Spinocerebellar ataxia type 17 Huntington disease-like 2 National Organization for Rare Disorders (NORD) ...
    https://medlineplus.gov/genetics/condition/huntingtons-disease-like - Genetics
  4. Myoclonic epilepsy myopathy sensory ataxia 
    ... SCAE Spinocerebellar ataxia with epilepsy ... variable tissue expression: a novel genetic abnormality in mitochondrial diseases. Am J Hum Genet. 1991 Mar;48(3): ...
    https://medlineplus.gov/...yoclonic-epilepsy-myopathy-sensory-ataxia - Genetics
  5. Friedreich ataxia 
    ... Friedreich ataxia often have a form of heart disease called hypertrophic cardiomyopathy, ... Genetic Testing Registry: Friedreich ...
    https://medlineplus.gov/genetics/condition/friedreich-ataxia - Genetics
  6. X-linked sideroblastic anemia and ataxia 
    ... spinocerebellar ataxia National ... anaemia with ataxia: another mitochondrial disease? J Neurol Neurosurg Psychiatry. 2001 Jan;70(1): ...
    https://medlineplus.gov/.../x-linked-sideroblastic-anemia-and-ataxia - Genetics
  7. Autosomal recessive cerebellar ataxia type 1 
    ... National Organization for Rare Disorders (NORD) ... ataxia with SYNE1 mutation accompanying motor neuron disease. Neurology. 2013 Feb 5;80(6):600-1. ...
    https://medlineplus.gov/...osomal-recessive-cerebellar-ataxia-type-1 - Genetics
  8. Ataxia with oculomotor apraxia 
    ... raise a person's risk of developing heart disease.Ataxia with oculomotor apraxia type 2 ... SCAR1 Spinocerebellar ataxia with axonal neuropathy type 2 Spinocerebellar ataxia, ...
    https://medlineplus.gov/.../condition/ataxia-with-oculomotor-apraxia - Genetics
  9. Primary coenzyme Q10 deficiency 
    Primary coenzyme Q10 deficiency is a disorder that can affect many parts of the body, especially the brain, muscles, and kidneys. As its name suggests, the disorder ...
    https://medlineplus.gov/.../primary-coenzyme-q10-deficiency - Genetics