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445 Possible Causes for Ataxia is Slowly Progressive

  • Unverricht-Lundborg Syndrome

    […] myoclonic and generalized seizures, ATAXIA, slowly progressive intellectual deterioration… (More) National Institutes of Health[] An autosomal recessive condition characterized by recurrent myoclonic and generalized seizures, ATAXIA, slowly progressive intellectual deterioration, dysarthria, and intention[] Known as: EPILEPSY, PROGRESSIVE MYOCLONIC, 1, EPILEPSY, PROGRESSIVE MYOCLONIC, 1A, Mediterranean Myoclonic Epilepsy An autosomal recessive condition characterized by recurrent[]

  • Peripheral Neuropathy

    Here, we report a Han Chinese family with SCA18; the family members presented with a slowly progressing gait ataxia, pyramidal tract signs, and peripheral neuropathy.[]

  • Spinocerebellar Ataxia Type 15

    Spinocerebellar ataxia 15 (SCA15) is a clinically heterogeneous movement disorder characterized by the adult onset of slowly progressive cerebellar ataxia..[] Spinocerebellar ataxia type 15 (SCA15), first described in 2001, is a slowly progressive, relatively pure dominantly inherited ataxia.[] Patients with nonprogressive or slowly progressive ataxia should be screened for ITPR1 defects. Actions (Repository Editors) Item Control Page[]

  • Spinocerebellar Ataxia Type 14

    In conclusion, the H101Q mutation causes slowly progressive uncomplicated ataxia by interfering with PKCgamma stability or solubility, which consequently may cause in either[] CLINICAL CHARACTERISTICS: Spinocerebellar ataxia type 14 (SCA14) is characterized by slowly progressive cerebellar ataxia, dysarthria, and nystagmus.[] In addition to slowly progressive cerebellar ataxia, it is characterised by dystonia and myoclonus.[]

  • Hemochromatosis

    A patient is reported with hereditary haemochromatosis and a syndrome of dementia, dysarthria, a slowly progressive gait disturbance, imbalance, muscle weakness, rigidity,[] […] bradykinesia, tremor, ataxia, and dyssynergia.[]

  • Spinocerebellar Ataxia Type 6

    Spinocerebellar ataxia type 6 (SCA6) is an autosomal dominant, slowly progressive cerebellar ataxia without multisystem involvement.[] BACKGROUND: Spinocerebellar ataxia type 6 (SCA6) is a neurodegenerative disorder characterized by slowly progressive ataxia and dysarthria.[] OBJECTIVE: Spinocerebellar ataxia type 6 (SCA6) is a neurodegenerative disorder characterized by a slowly progressive ataxia and dysarthria. Anatomically.[]

  • Hereditary Late-Onset Parkinson Disease

    The symptoms begin in later adulthood and appear to progress more slowly than other types of ataxia.[] Spinocerebellar Ataxias are a group of progressive degenerative inherited conditions characterized by slowly progressive incoordination of hands, speech, eye movements and[] This type of ataxia appears to be a slowly progressive form of ataxia. Symptoms may begin as early as childhood, or as late as the 60’s.[]

  • Cerebellar Stroke

    When diagnosing ACA in adults, doctors first try to distinguish ACA from other types of cerebellar ataxias that come on more slowly.[] Causes are often similar to ACA, but subacute ataxias are also caused by rare infections such as prion diseases , Whipple’s disease , and progressive multifocal leukoencephalopathy[] Sometimes subacute ataxias can seem to come on quickly, but in reality, they have been developing slowly over time.[]

  • 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.[] CLINICAL CHARACTERISTICS: In the families described to date, the phenotype of spinocerebellar ataxia type 13 (SCA13) has ranged from slowly progressive childhood-onset cerebellar[] 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[]

  • X-linked Parkinsonism-Spasticity Syndrome

    Ataxia can occur suddenly (acute), over weeks (subacute) or slowly progressive over months to years (chronic).[]

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