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3,083 Possible Causes for Cerebellar Ataxia, Loss of Ambulation between Third and Sixth Decade, Persistent Notochordal Canal

  • Limb-Girdle Muscular Dystrophy Type 2J

    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] notochordal canal syndrome Salla disease Salt-and-pepper syndrome Sandhoff disease Sandhoff disease, adult form Sandhoff disease, infantile form Sandhoff disease, juvenile[se-atlas.de] […] recessive cerebellar ataxia due to a DNA repair defect Autosomal recessive cerebellar ataxia with late-onset spasticity Autosomal recessive cerebellar ataxia-epilepsy-intellectual[se-atlas.de]

  • Myelocerebellar Disorder

    Ataxia-pancytopenia (AP) syndrome is seen as a cerebellar ataxia, variable hematologic cytopenias, and predisposition to marrow failing and myeloid leukemia, connected with[hiv-proteases.com] notochordal canal syndrome Salla disease Salt-and-pepper syndrome Sandhoff disease Sandhoff disease, adult form Sandhoff disease, infantile form Sandhoff disease, juvenile[se-atlas.de] […] disorders in cerebellar ataxia were not treatable.[en.wikipedia.org]

    Missing: Loss of Ambulation between Third and Sixth Decade
  • Infantile-Onset Autosomal Recessive Nonprogressive Cerebellar Ataxia

    Applicable To Early-onset cerebellar ataxia with essential tremor Early-onset cerebellar ataxia with myoclonus [Hunt's ataxia] Early-onset cerebellar ataxia with retained[icd10data.com] notochordal canal syndrome Salla disease Salt-and-pepper syndrome Sandhoff disease Sandhoff disease, adult form Sandhoff disease, infantile form Sandhoff disease, juvenile[se-atlas.de] The Blueprint Genetics ataxia panel covers classical genes associated with cerebellar ataxia, spinocerebellar ataxia and episodic ataxia.[blueprintgenetics.com]

    Missing: Loss of Ambulation between Third and Sixth Decade
  • Congenital Non-Progressive Ataxia

    Since that time the syndrome of cerebellar ataxia, oligophrenia, and congenital cataracts has become known as the Marinesco-Sjogren syndrome.[doi.org] notochordal canal syndrome Salla disease Salt-and-pepper syndrome Sandhoff disease Sandhoff disease, adult form Sandhoff disease, infantile form Sandhoff disease, juvenile[se-atlas.de] Non-progressive cerebellar ataxia is associated with delayed developmental milestones and hypotonia (visible from the first year of life), gait and balance disorders with[orpha.net]

    Missing: Loss of Ambulation between Third and Sixth Decade
  • Chronic Alcoholism

    There was a progressive development of parkinsonism, cerebellar ataxia, and mental deterioration by the time he was 32.[ncbi.nlm.nih.gov] Others develop for non-hereditary reasons, such as alcoholic cerebellar ataxia. What Is Cerebellar Ataxia? Cerebellar ataxia is a symptom, not a distinct disorder.[promises.com] * Affects nearly every organ system: NEURO – Affects both peripheral nervous system (peripheral neuropathy) and central nervous sytem : Cognitive dysfunction, Cerebellar degeneration[errolozdalga.com]

    Missing: Loss of Ambulation between Third and Sixth Decade Persistent Notochordal Canal
  • Lower Motor Neuron Syndrome with Late-Adult Onset

    The authors describe six new late-onset Sandhoff cases demonstrating cerebellar ataxia or lower motor neuron (LMN) involvement combined with, mostly subclinical, neuropathy[ncbi.nlm.nih.gov] notochordal canal syndrome Salla disease Salt-and-pepper syndrome Sandhoff disease Sandhoff disease, adult form Sandhoff disease, infantile form Sandhoff disease, juvenile[se-atlas.de] G11.1 Early-onset cerebellar ataxia G11.2 Late-onset cerebellar ataxia G11.3 Cerebellar ataxia with defective DNA repair G11.4 Hereditary spastic paraplegia G11.8 Other hereditary[icd10data.com]

    Missing: Loss of Ambulation between Third and Sixth Decade
  • Infectious Mononucleosis

    Infectious mononucleosis (IM) complicated with a neurological manifestation, including acute cerebellar ataxia, Guillain-Barre syndrome, meningitis, encephalitis, cranial[ncbi.nlm.nih.gov] Ataxia Guillain-Barre syndrome Pancreatitis Myocarditis Pneumonia Lung disease Lymphocytosis Weakened immune system To find out more about these other possible illnesses,[americanpregnancy.org] ataxia. 4 The role of plasmapheresis in treating Guillain—Barré variants is not clear.[nejm.org]

    Missing: Loss of Ambulation between Third and Sixth Decade Persistent Notochordal Canal
  • Hypothyroidism

    Rarely it can present with neurologic problems like reversible cerebellar ataxia, dementia, peripheral neuropathy, psychosis and coma.[ncbi.nlm.nih.gov] Cerebellar ataxia. Psychosis. Encephalopathy. Patients can go on to develop myxoedema coma (see below).[patient.info] Hypothyroidism should be considered in all cases of cerebellar ataxia as it is a reversible cause of ataxia. [Indexed for MEDLINE] Free full text[ncbi.nlm.nih.gov]

    Missing: Loss of Ambulation between Third and Sixth Decade Persistent Notochordal Canal
  • Strabismus

    […] autosomal dominant cerebellar ataxia type 1, characterized by the adult-onset of unsteady gait and dysarthria, followed by wide-based gait, gait ataxia, ocular dysmetria,[orpha.net] These patients presented with a form of cerebellar ataxia with slow saccadic eye movements4.[scielo.br] Keywords: Spinocerebellar ataxia, ataxic dysarthria, perceptual analysis, acoustic analysis, cerebellar degenerative disorders, cognitive impairment, language impairment,[openarchive.ki.se]

    Missing: Loss of Ambulation between Third and Sixth Decade Persistent Notochordal Canal
  • Oculo-Palato-Cerebral Syndrome

    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] ataxia with intellectual disability 15 Cases 363494 Non-seminomatous germ cell tumor of testis 1.21 I * 90031 Non-spherocytic hemolytic anemia due to hexokinase deficiency[azkurs.org] cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to WWOX[se-atlas.de]

    Missing: Loss of Ambulation between Third and Sixth Decade

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