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5,350 Possible Causes for Ataxia, Progressive Disease

  • Primary Progressive Multiple Sclerosis

    Spastic paraparesis and progressive ataxia are principal symptoms in this subset of patients.[symptoma.com] The majority of patients starts with relapsing remitting (RR) disease; approximately 50-60% of these patients progress to secondary progressive (SP) disease.[ncbi.nlm.nih.gov] Abstract HDLS (Hereditary Diffuse Leukodystrophy with Spheroids) is a hereditary leukodystrophy whose main clinical manifestations include parkinsonism, spasticity, and ataxia[ncbi.nlm.nih.gov]

  • Progressive Supranuclear Palsy

    His principal symptom was cerebellar ataxia for several years.[ncbi.nlm.nih.gov] The current gold standard for measuring clinical disease progression in PSP is the PSP Rating Scale score.[ncbi.nlm.nih.gov] Some of the main symptoms of MSA, such as cerebellar ataxia and orthostatic hypotension, are not rare parts of the clinical picture of PSP.[ncbi.nlm.nih.gov]

  • Lafora Disease

    Cerebellar ataxia and/or involuntary movements Epidemiology Transmitted in an autosomal recessive fashion.[wiki.med.umich.edu] Daily living activities and social interaction were preserved in all cases and, overall, the progression of the disease was slow.[ncbi.nlm.nih.gov] Lafora disease (LD), also known as progressive myoclonic epilepsy-2 (EPM2), is a rare, fatal autosomal recessive disorder typically starting during adolescence in otherwise[ncbi.nlm.nih.gov]

  • Amyotrophic Lateral Sclerosis

    Blood from ND patients with PD, ALS and Ataxia with movement dysfunctions were obtained to analyse mRNA and protein expressions of the above mentioned factors in lymphocytes[ncbi.nlm.nih.gov] This review examined current research related to moderate exercise for maintaining independence without accelerating disease progression in persons with ALS.[ncbi.nlm.nih.gov] A 75-year-old female patient presented with cerebellar ataxia, bulbar palsy and cognitive impairment.[ncbi.nlm.nih.gov]

  • Unverricht-Lundborg Syndrome

    Creutzfeldt-Jakob disease classically presents with rapidly progressive cerebellar ataxia and myoclonus, as well as dementia and sometimes cortical visual disturbances.[aibolita.com] This disease is classified as a type of progressive myoclonus epilepsy.[ivami.com] Read More About Neuroimmunology & Neuroinflammation Clinical Reasoning: Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy ... decline, neuropathy[aan.com]

  • Progressive Myoclonic Epilepsy Type 3

    Dentatorubral-pallidoluysian atrophy  Rare autosomal-dominant neurodegenerative disorder, characterised by various combinations of cerebellar ataxia, choreoathetosis, myoclonus[slideshare.net] […] gene sharing: Search GEO for disease gene expression data for Epilepsy Progressive Myoclonic Type 3.[malacards.org] Clinical manifestations of the patients include cerebellar ataxia with myopathy, recurrent headache, and myoclonus and epilepsy....[connection.ebscohost.com]

  • Niemann-Pick Disease Type C

    ataxia, vertical supranuclear gaze palsy (VSPG), dysarthria, dysphagia, dystonia, seizures, gelastic cataplexy, and psychiatric disorders.[orpha.net] An NP-C-specific disability scale was used to measure disease progression.[ncbi.nlm.nih.gov] Vertical supranuclear gaze palsy, cerebellar ataxia, dementia, dystonia and dysarthria were present in all cases.[ncbi.nlm.nih.gov]

  • Progressive Myoclonic Epilepsy Type 7

    Dentatorubral-pallidoluysian atrophy  Rare autosomal-dominant neurodegenerative disorder, characterised by various combinations of cerebellar ataxia, choreoathetosis, myoclonus[slideshare.net] : Search GEO for disease gene expression data for Epilepsy Progressive Myoclonic Type 3.[malacards.org] ataxia Autosomal dominant cerebellar ataxia type I Autosomal dominant cerebellar ataxia type II Autosomal dominant cerebellar ataxia type III Autosomal dominant cerebellar[se-atlas.de]

  • Huntington's Disease

    We screened 89 patients with a Huntington's disease-like phenotype without the HD-gene mutation and 178 patients with genetically unclassified cerebellar ataxia for the mutation[ncbi.nlm.nih.gov] HD is a progressive disease; this means that it gets worse over time, and coordination of everyday activities become harder and harder.[my.clevelandclinic.org] The authors highlight the importance of suspecting HD in the aetiology of spinocerebellar ataxias when dementia is a prominent feature in the proband or their family.[ncbi.nlm.nih.gov]

  • Progressive Myoclonic Epilepsy Type 8

    Category Nervous system disease Brite Human diseases [BR: br08402 ] Nervous system diseases Epilepsy H00810 Progressive myoclonic epilepsy Human diseases in ICD-11 classification[genome.jp] Friedreich's ataxia, spinocerebellar ataxias types 1, 2, 3, 6, 7, 12, 17 and dentatorubropallidoluysian atrophy molecular analysis came out negative.[onlinelibrary.wiley.com] A type of progressive myoclonic epilepsy, Lafora disease: A case report. Eastern J Med. 2013; 18(1): 34-36[eastjmed.org]

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