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33 Possible Causes for Cerebellar Disease, Neuronal Loss and Gliosis in the Inferior Olives

  • Olivopontocerebellar Atrophy

    These findings suggest important pathophysiological roles of cerebellin and CRH in these cerebellar diseases.[ncbi.nlm.nih.gov] There is neuronal loss and gliosis in the inferior olives, pons, cerebellum, substantia nigra, locus ceruleus, striatum and the intermediolateral column of the spinal cord[dizziness-and-balance.com] Microscopic examination of these structures reveals neuronal loss, axon and myelin degeneration, and gliosis.[neuropathology-web.org]

  • Hereditary Cerebellar Degeneration

    To Hereditary cerebellar ataxia NOS Hereditary cerebellar degeneration Hereditary cerebellar disease Hereditary cerebellar syndrome in specified disease NEC G32.81 ICD-10[icd10data.com] Microscopic examination of these structures reveals neuronal loss, axon and myelin degeneration, and gliosis.[neuropathology-web.org] 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]

  • Friedreich Ataxia

    Ataxia Friedreich Ataxia Dyskinesias Neurologic Manifestations Nervous System Diseases Signs and Symptoms Cerebellar Diseases Brain Diseases Central Nervous System Diseases[clinicaltrials.gov] Microscopic examination of these structures reveals neuronal loss, axon and myelin degeneration, and gliosis.[neuropathology-web.org] Last Verified: February 2019 Individual Participant Data (IPD) Sharing Statement: Plan to Share IPD: No Additional relevant MeSH terms: Layout table for MeSH terms Ataxia Cerebellar[clinicaltrials.gov]

  • Cerebellar Ataxia

    To Hereditary cerebellar ataxia NOS Hereditary cerebellar degeneration Hereditary cerebellar disease Hereditary cerebellar syndrome in specified disease NEC G32.81 ICD-10[icd10data.com] Microscopic examination of these structures reveals neuronal loss, axon and myelin degeneration, and gliosis.[neuropathology-web.org] cerebellar ataxia cerebellar disease characterized by ataxia originating in the cerebellum.[wikidata.org]

  • Ataxia

    Bastian, Longitudinal tracking of gait and balance impairments in cerebellar disease, Movement Disorders, 25, 12, (1944-1952), (2010).[doi.org] Microscopic examination of these structures reveals neuronal loss, axon and myelin degeneration, and gliosis.[neuropathology-web.org] In addition, mild secondary neuronal cell loss with gliosis was noted in the dentate nucleus and inferior olive.[jneuroinflammation.com]

  • Cerebellar Ataxia with Peripheral Neuropathy Type 2

    […] for balance control in cerebellar disease 2008 National College of Occupational Therapists Conference, Newcastle Vestibular processing for balance control in cerebellar disease[www6.plymouth.ac.uk] Microscopic examination of these structures reveals neuronal loss, axon and myelin degeneration, and gliosis.[neuropathology-web.org] Entries on cerebellar diseases, peripheral neuropathies, various dementias, diagnostic tests (both clinical and laboratory), forms of cerebral edema, dissociative signs and[books.google.com]

  • Adult-Onset Autosomal Recessive Cerebellar Ataxia

    To Hereditary cerebellar ataxia NOS Hereditary cerebellar degeneration Hereditary cerebellar disease Hereditary cerebellar syndrome early-onset G11.1 hereditary G11.9 ICD[icd10data.com] Microscopic examination of these structures reveals neuronal loss, axon and myelin degeneration, and gliosis.[neuropathology-web.org] […] duration - Gaze-evoked nystagmus Patients with longer disease duration - Dysmetric saccades, slow saccades, ophthalmoparesis, and ptosis Cerebellar atrophy Spinocerebellar[emedicine.medscape.com]

  • Autosomal Recessive Spinocerebellar Ataxia 8

    To Hereditary cerebellar ataxia NOS Hereditary cerebellar degeneration Hereditary cerebellar disease Hereditary cerebellar syndrome early-onset G11.1 hereditary G11.9 ICD[icd10data.com] Microscopic examination of these structures reveals neuronal loss, axon and myelin degeneration, and gliosis.[neuropathology-web.org] […] duration - Gaze-evoked nystagmus Patients with longer disease duration - Dysmetric saccades, slow saccades, ophthalmoparesis, and ptosis Cerebellar atrophy Spinocerebellar[emedicine.medscape.com]

  • Autosomal Recessive Spinocerebellar Ataxia

    To Hereditary cerebellar ataxia NOS Hereditary cerebellar degeneration Hereditary cerebellar disease Hereditary cerebellar syndrome early-onset G11.1 hereditary G11.9 ICD[icd10data.com] Microscopic examination of these structures reveals neuronal loss, axon and myelin degeneration, and gliosis.[neuropathology-web.org] […] duration - Gaze-evoked nystagmus Patients with longer disease duration - Dysmetric saccades, slow saccades, ophthalmoparesis, and ptosis Cerebellar atrophy Spinocerebellar[emedicine.medscape.com]

  • Spinocerebellar Ataxia Type 5

    Among those examined, 56 individuals have a generally non-life threatening cerebellar ataxia. Disease onset varies from 10-68 years and anticipation is evident.[ncbi.nlm.nih.gov] loss and gliosis.[link.springer.com] […] ataxia NOS Hereditary cerebellar degeneration Hereditary cerebellar disease Hereditary cerebellar syndrome specified NEC G11.8 Disease, diseased - see also Syndrome spinocerebellar[icd10data.com]

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