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36 Possible Causes for Huntington's Disease, Onset of Dysarthria in Third Decade of Life

  • Spinocerebellar Ataxia Type 1

    […] in third to fifth decade of life Pure cerebellar ataxia, nystagmus, dysarthria, dysphagia, hypotonia, and generalized and/or complex partial epilepsy Spinocerebellar ataxia[emedicine.com] […] and Huntington’s disease.[doi.org] Clinical trials of neural transplants in Huntington's disease patients are under way.[ncbi.nlm.nih.gov]

  • Hallervorden-Spatz Syndrome

    In this respect, HSS may serve as a model for complex neurodegenerative diseases, such as Parkinson disease, Alzheimer disease, Huntington disease and human immunodeficiency[ncbi.nlm.nih.gov] Clinical features Dystonia Dysarthria Spasticity Choreoathetosis Parkinsonism Hyperreflexia Extensor toe signs Onset in first to third decade of life Gait change / loss of[ncbi.nlm.nih.gov] disease.[ncbi.nlm.nih.gov]

  • Autosomal Recessive Spinocerebellar Ataxia Type 17

    The Huntington’s disease-like syndromes: what to consider in patients with a negative Huntington’s disease gene test.[ncbi.nlm.nih.gov] […] in third to fifth decade of life Pure cerebellar ataxia, nystagmus, dysarthria, dysphagia, hypotonia, and generalized and/or complex partial epilepsy Spinocerebellar ataxia[emedicine.medscape.com] Disease-Like Syndromes Huntington's disease-like disorders are a rare cause of chorea (Table 1 ).[movementdisorders.org]

  • Spinocerebellar Ataxia Type 6

    Alternatively, as a disease in which the mutant protein contains an expanded polyglutamine tract, SCA6 may respond to the targets of drug therapies developed for Huntington's[ncbi.nlm.nih.gov] […] in third to fifth decade of life Pure cerebellar ataxia, nystagmus, dysarthria, dysphagia, hypotonia, and generalized and/or complex partial epilepsy Spinocerebellar ataxia[emedicine.com] Calcium channel Cerebellum Episodic ataxia Familial hemiplegic migraine Huntington's disease Spinocerebellar ataxia sca6 at NIH/UW GeneTests[en.wikipedia.org]

  • Adult-Onset Autosomal Recessive Cerebellar Ataxia

    […] in third to fifth decade of life Pure cerebellar ataxia, nystagmus, dysarthria, dysphagia, hypotonia, and generalized and/or complex partial epilepsy Spinocerebellar ataxia[emedicine.medscape.com] […] been recognized as a "Center of Excellence" by the National Parkinson Foundation and the Huntington Disease Society of America.[books.google.com] CoQ10 has shown efficacy in treatment of Parkinson's disease patients, and a Huntington's disease trial gave a trend of slowing down disease progression (CARE-HD).[clinicaltrials.gov]

  • Spinocerebellar Ataxia with Axonal Neuropathy

    , Huntington's disease, dystonia, tremors, and tics[books.google.com] […] in third to fifth decade of life Pure cerebellar ataxia, nystagmus, dysarthria, dysphagia, hypotonia, and generalized and/or complex partial epilepsy Spinocerebellar ataxia[emedicine.medscape.com] […] been recognized as a "Center of Excellence" by the National Parkinson Foundation and the Huntington Disease Society of America.[books.google.com]

  • Spinocerebellar Ataxia Type 4

    (HDL4: Huntington Disease-like type 4), is a disorder resembling Huntington's disease.[ivami.com] […] in third to fifth decade of life Pure cerebellar ataxia, nystagmus, dysarthria, dysphagia, hypotonia, and generalized and/or complex partial epilepsy Spinocerebellar ataxia[emedicine.medscape.com] […] been recognized as a "Center of Excellence" by the National Parkinson Foundation and the Huntington Disease Society of America.[books.google.es]

  • Autosomal Recessive Spinocerebellar Ataxia

    An internationally recognized authority on neurodegenerative disorders, his research has focused on the mechanism of neuronal degeneration in Alzheimer's disease, Huntington's[books.google.com] […] in third to fifth decade of life Pure cerebellar ataxia, nystagmus, dysarthria, dysphagia, hypotonia, and generalized and/or complex partial epilepsy Spinocerebellar ataxia[emedicine.medscape.com] Similar to Huntington’s disease (which is also caused by CAG repeats), the ADSCAs show the phenomenon of anticipation, i.e. lengthening of the CAG repeat with earlier onset[neuropathology-web.org]

  • Autosomal Recessive Spastic Ataxia with Leukoencephalopathy

    The Huntington's disease-like syndromes: what to consider in patients with a negative Huntington's disease gene test. Nat Clin Pract Neurol. 2007;3(9):517-25.[books.google.es] […] in third to fifth decade of life Pure cerebellar ataxia, nystagmus, dysarthria, dysphagia, hypotonia, and generalized and/or complex partial epilepsy Spinocerebellar ataxia[emedicine.medscape.com] , frontotemporal dementias, Huntington's disease, prionoses) and other common neurological disorders that may be complicated by cognitive impairment (stroke, multiple sclerosis[books.google.com]

  • Spinocerebellar Ataxia Type 5

    […] and Huntington diseases, SCA1 and ALS.[ashg.org] The onset of symptoms is usually in the third or fourth decade of life; however, more subtle clinical manifestations can start in early childhood.[ncbi.nlm.nih.gov] Motor disruption also occurs in Huntington's disease (HD), a genetic disorder that causes degeneration of brain cells in certain areas of the brain, resulting in uncontrolled[rxpgnews.com]

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