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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[semanticscholar.org] An autosomal recessive condition characterized by recurrent myoclonic and generalized seizures, ATAXIA, slowly progressive intellectual deterioration, dysarthria, and intention[rareomics.healx.io] Known as: EPILEPSY, PROGRESSIVE MYOCLONIC, 1, EPILEPSY, PROGRESSIVE MYOCLONIC, 1A, Mediterranean Myoclonic Epilepsy An autosomal recessive condition characterized by recurrent[semanticscholar.org]

  • 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.[ncbi.nlm.nih.gov]

  • Spinocerebellar Ataxia Type 15

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

  • 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[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] In addition to slowly progressive cerebellar ataxia, it is characterised by dystonia and myoclonus.[ncbi.nlm.nih.gov]

  • Hemochromatosis

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

  • Spinocerebellar Ataxia Type 6

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

  • Hereditary Late-Onset Parkinson Disease

    The symptoms begin in later adulthood and appear to progress more slowly than other types of ataxia.[ataxiacenter.umn.edu] Spinocerebellar Ataxias are a group of progressive degenerative inherited conditions characterized by slowly progressive incoordination of hands, speech, eye movements and[dystonia-parkinsons.org] 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.[ataxiacenter.umn.edu]

  • Cerebellar Stroke

    When diagnosing ACA in adults, doctors first try to distinguish ACA from other types of cerebellar ataxias that come on more slowly.[healthline.com] 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[healthline.com] Sometimes subacute ataxias can seem to come on quickly, but in reality, they have been developing slowly over time.[healthline.com]

  • 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]

  • X-linked Parkinsonism-Spasticity Syndrome

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

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