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217 Possible Causes for Broad-Based Gait, Cerebellar Disease

  • Cerebellar Disease

    Results are discussed in terms of the effects of cerebellar disease on neuromuscular function.[ncbi.nlm.nih.gov] No- differentiates a cerebellar broad based gait from a sensory broad based gait. How is the speech in cerebellar syndrome described?[brainscape.com] OPCA Toxic/metabolic diseases Hypothyroidism & normal pressure hydrocephalus Ataxic Dysarthria: Neuromotor Deficits Hypotonia and reduced resistance to passive movement Broad-based[ucs.louisiana.edu]

  • Acute Cerebellar Ataxia

    Four previously published reports of cerebellar ataxia with Lyme disease are reviewed.[pediatricneurologybriefs.com] In contrast, there are few reports of cerebellar involvement in pediatric Lyme disease patients.[ncbi.nlm.nih.gov] Applicable To Hereditary cerebellar ataxia NOS Hereditary cerebellar degeneration Hereditary cerebellar disease Hereditary cerebellar syndrome in specified disease NEC G32.81[icd10data.com]

  • Ataxia Telangiectasia

    Applicable To Hereditary cerebellar ataxia NOS Hereditary cerebellar degeneration Hereditary cerebellar disease Hereditary cerebellar syndrome with defective DNA repair G11.3[icd10data.com] AT is a neurodegenerative disease primarily characterized by cerebellar degeneration in children leading to motor impairment.[ncbi.nlm.nih.gov] Hallmarks of the disease comprise progressive cerebellar ataxia, oculocutaneous telangiectasiae, cancer susceptibility, and variable humoral and cellular immunodeficiency.[ncbi.nlm.nih.gov]

  • Friedreich Ataxia

    Applicable To Hereditary cerebellar ataxia NOS Hereditary cerebellar degeneration Hereditary cerebellar disease Hereditary cerebellar syndrome early-onset G11.1 hereditary[icd10data.com] Disease severity and genetic markers of disease liability were correlated specifically with cerebellar dysfunction, while correlations between behavioural performance and[ncbi.nlm.nih.gov] […] degeneration Hereditary cerebellar disease Hereditary cerebellar syndrome spinal G11.1 (Friedreich's) spinal hereditary G11.1 (Friedreich's) Friedreich's G11.1 (heredofamilial[icd10data.com]

  • Hereditary Areflexic Dystasia

    Azorean disease, type I Azorean disease, type III Azorean disease, type IV Cerebellar ataxia Cerebellar ataxia (loss of muscle coordination) Cerebellar ataxia due to toxin[icd9data.com] Roussy-Lévy disease [roo͡sē′ lāvē′] Etymology: Gustave Roussy, French pathologist, 1874-1948; Gabrielle Lévy, French neurologist, 1886-1935 an inherited cerebellar ataxia[medical-dictionary.thefreedictionary.com] Convert to ICD-10-CM : 334.3 converts approximately to: 2015/16 ICD-10-CM G11.1 Early-onset cerebellar ataxia Approximate Synonyms Abortive cerebellar ataxia Azorean disease[icd9data.com]

  • Spinocerebellar Ataxia Type 1

    "Cerebellar Ataxia Rehabilitation Trial in Degenerative Cerebellar Diseases". Neurorehabilitation and Neural Repair . 26 (5): 515–22. doi : 10.1177/1545968311425918 .[en.wikipedia.org] There is a broad-based gait, scanning dysarthria, explosive speech, intention tremor, dysdiadochokinesia, dysmetria and abnormalities of eye movements.[patient.info] […] ataxia NOS Hereditary cerebellar degeneration Hereditary cerebellar disease Hereditary cerebellar syndrome specified NEC G11.8 Disease, diseased - see also Syndrome spinocerebellar[icd10data.com]

  • Hereditary Cerebellar Degeneration

    Applicable To Hereditary cerebellar ataxia NOS Hereditary cerebellar degeneration Hereditary cerebellar disease Hereditary cerebellar syndrome in specified disease NEC G32.81[icd10data.com] There is a broad-based gait, scanning dysarthria, explosive speech, intention tremor, dysdiadochokinesia, dysmetria and abnormalities of eye movements.[patient.info] These studies suggest that patients with cerebellar diseases may benefit from screening and treatment of psychiatric disorders . [2] Last updated: 12/14/2014 How might cerebellar[rarediseases.info.nih.gov]

  • Diabetic Pseudotabes

    Entries on cerebellar diseases, peripheral neuropathies, various dementias, diagnostic tests (both clinical and laboratory), forms of cerebral edema, dissociative signs and[books.google.com] In addition to the broad-based, stamping gait, which becomes worse when patients try to walk in the dark, abnormal findings included diminished vision owing to optic atrophy[std-aid.com] disease: posterior fossa tumours: acoustic neuroma 1 cerebellar tumours metastases degenerative cerebellar disease: hereditary: ataxia-telangiectasia Friedreich's ataxia[sinoemedicalassociation.org]

  • Alcoholic Cerebellar Degeneration

    Thirty-two patients (49%) had clear clinical signs of the disease such as broad-based staggering gait, impaired heel-to-toe walking, terminal oscillations in heel-knee test[ncbi.nlm.nih.gov] Stance – a broad-based gait is noted in cerebellar disease 2.[geekymedics.com] Clinical manifestations evolve over months to years and include truncal instability, broad-based stance and gait ataxia.[urmc.rochester.edu]

  • Hereditary Sensory Neuropathy

    Entries on cerebellar diseases, peripheral neuropathies, various dementias, diagnostic tests (both clinical and laboratory), forms of cerebral edema, dissociative signs and[books.google.de] They tend to have broad-based gaits and ataxia issues that worsen with age.[medicalbag.com] In the second edition further precision in definition has been achieved for the entries on at least 1,500 other disease states, syndromes, and clinical features.[books.google.de]

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