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285 Possible Causes for Slowly Progressive Cerebellar Ataxia

  • Spinocerebellar Ataxia Type 14

    In addition to slowly progressive cerebellar ataxia, it is characterised by dystonia and myoclonus.[ncbi.nlm.nih.gov] All affected patients had slowly progressive cerebellar ataxia frequently associated with brisk reflexes.[ncbi.nlm.nih.gov] CLINICAL CHARACTERISTICS: Spinocerebellar ataxia type 14 (SCA14) is characterized by slowly progressive cerebellar ataxia, dysarthria, and nystagmus.[ncbi.nlm.nih.gov]

  • Spinocerebellar Ataxia Type 15

    All patients with SCA15 (n 10) presented with slowly progressive cerebellar ataxia and vermal cerebellar atrophy, while clinical and electrophysiological signs of extracerebellar[ncbi.nlm.nih.gov] progressive cerebellar ataxia..[mayoclinic.pure.elsevier.com] Screening for ITPR1 deletions should be considered in patients with slowly progressive SCA, vermal cerebellar atrophy and prominent tremor after excluding common SCA repeat[jmg.bmj.com]

  • Oculomotor Apraxia

    Abstract Ataxia with oculomotor apraxia type 1 (AOA1) is an autosomal recessive disease characterized by early-onset and slowly progressive cerebellar ataxia, areflexia, and[ncbi.nlm.nih.gov] BACKGROUND: Ataxia with oculomotor apraxia type 1 is an autosomal-recessive neurodegenerative disorder characterized by a childhood onset of slowly progressive cerebellar[ncbi.nlm.nih.gov] progressive cerebellar ataxia, which usually presents with gait ataxia (3) oculomotor apraxia that progresses to an external ophthalmoplegia (4) axonal motor polyneuropathy[meducator3.net]

  • Spinocerebellar Ataxia with Axonal Neuropathy

    Spinocerebellar ataxia with axonal neuropathy type 1 is a rare, genetic neurological disorder characterized by a late childhood onset of slowly progressive cerebellar ataxia[monarchinitiative.org] Spinocerebellar ataxia with axonal neuropathy (SCAN1) is characterized by late childhood-onset of a slowly progressive cerebellar ataxia, followed by areflexia and signs of[healthetreatment.com] […] apraxia (AOA) is a rare inherited disease characterized by childhood onset of slowly progressive cerebellar ataxia, followed by oculomotor apraxia and a severe primary motor[centogene.com]

  • Cerebellar Ataxia

    All of the patients described here showed very slowly progressive cerebellar ataxia and cognitive decline with choreiform involuntary movement, with young adolescent or midlife[ncbi.nlm.nih.gov] We collected 346 consecutive patients with the core features of the criteria (sporadic, insidious-onset and slowly progressive cerebellar ataxia in adults, and cerebellar[ncbi.nlm.nih.gov] Many of these causes of ataxia are treatable. Most slowly progressive cerebellar ataxias result from neurodegenerative aetiologies, either inherited or sporadic.[els.net]

  • Spinocerebellar Ataxia Type 6

    Spinocerebellar ataxia type 6 (SCA6) is an autosomal dominant, slowly progressive cerebellar ataxia without multisystem involvement.[ncbi.nlm.nih.gov] SCA-6 is characterized predominantly by slowly progressive pure cerebellar ataxia with late onset.[ncbi.nlm.nih.gov] SCA6 is a slowly progressive, late-onset cerebellar ataxia due to a trinucleotide expansion in the CACNA1A gene.[ncbi.nlm.nih.gov]

  • Spinocerebellar Ataxia Type 13

    All affected family members had a slowly progressive cerebellar ataxia, with an age of onset range from 26 to 60 years.[experts.umn.edu] CLINICAL CHARACTERISTICS: In the families described to date, the phenotype of spinocerebellar ataxia type 13 (SCA13) has ranged from slowly progressive childhood-onset cerebellar[ncbi.nlm.nih.gov] The patients-seven women and a 4-year-old boy-exhibited slowly progressive childhood-onset cerebellar gait ataxia associated with cerebellar dysarthria, moderate mental retardation[childnervoussystem.blogspot.com]

  • Ataxia-Telangiectasia-Like Disorder Type 1

    The patient showed slowly progressive cerebellar ataxia from 2 years of age, and MRI revealed atrophy of the cerebellum, oculomotor apraxia, mild cognitive impairment, writing[pubfacts.com] […] apraxia (AOA) is a rare inherited disease characterized by childhood onset of slowly progressive cerebellar ataxia, followed by oculomotor apraxia and a severe primary motor[centogene.com] DISEASE CHARACTERISTICS: Ataxia with oculomotor apraxia type 1 (AOA1) is characterized by childhood onset of slowly progressive cerebellar ataxia, followed by oculomotor apraxia[lacaf.org]

  • Spinocerebellar Ataxia Type 19

    Affected individuals displayed a lateonset slowly progressive mild cerebellar ataxia, hyporeflexia, and signs of frontal lobe dysfunction.[ncbi.nlm.nih.gov] SCA-6 is characterized predominantly by slowly progressive pure cerebellar ataxia with late onset.[scielo.br] SCA 6 is traditionally described as a progressive, slowly, pure cerebellar ataxia with late onset.[scielo.br]

  • Myelocerebellar Disorder

    Neurologic features variably include slowly progressive cerebellar ataxia or balance impairment with cerebellar atrophy and periventricular white matter T2 hyperintensities[rarediseases.info.nih.gov] SYNDROME; ATXPC Ataxia-pancytopenia syndrome is a rare genetic disease characterized by cerebellar ataxia, cytopenias and predisposition to bone marrow failure and myeloid[mendelian.co] Orpha Number: 2585 Disease definition Ataxia -pancytopenia syndrome is a rare genetic disease characterized by cerebellar ataxia, cytopenias and predisposition to bone marrow[rarediseases.info.nih.gov]

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