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462 Possible Causes for Cerebellar Vermis Atrophy

  • Autosomal Recessive Spastic Ataxia Type Charlevoix-Saguenay

    Left—sagittal cut, T1-weighted sequence revealing cerebellar vermis atrophy (arrow).[frontiersin.org] Other common but less specific findings include 1-4 : inferior vermis atrophy superior spinal cord atrophy cerebellar hemisphere atrophy bulky pons with hypointense T2 stripe[radiopaedia.org] In the literature, early atrophy of the superior vermis as well as progressive atrophy of the cerebellar hemispheres and cervical cord was described.[ajnr.org]

  • Hypogonadotropic Hypogonadism 21

    On brain MRI relatively selective atrophy of the superior and dorsal parts of the cerebellar vermis along with atrophy of the cerebellar hemispheres was found in a substantial[neurology.org] […] patients and the previously published cases propose that the clinical presentation of BNS is variable regarding disease severity, age (range 1-40y) and clinical symptoms (cerebellar[neurology.org]

  • Hemiplegic Migraine

    A 10-year-old boy with psychomotor developmental delay and cerebellar vermis atrophy developed right hemiplegia with vomiting, unconsciousness, convulsions, and late-onset[ncbi.nlm.nih.gov] The MRI sequence reveals a cerebellar atrophy most pronounced in the vermis.[karger.com] Moreover, the MRI revealed enlarged Virchow-Robin spaces and cerebellar atrophy most pronounced in the vermis, a normal substantia nigra (SN), and only a few unspecific white[karger.com]

  • Wernicke-Korsakoff Syndrome

    […] of affected structures Gross images Images hosted on other servers : Cerebellar vermis atrophy not evident Microscopic (histologic) description Acute Wernicke encephalopathy[pathologyoutlines.com] […] or with intravenous glucose Gross description Acute Wernicke encephalopathy: hemorrhages in mammillary bodies, medial thalami, periaqueductal gray matter Chronic lesions: atrophy[pathologyoutlines.com]

  • Monoclonal Gammopathy of Undetermined Significance

    We report the case of a young man who had been suffering for five years of progressive cerebellar syndrome. MRI showed marked cerebellar vermis atrophy.[ncbi.nlm.nih.gov]

  • Autosomal Recessive Ataxia Type Beauce

    Brain imaging shows cerebellar atrophy mainly affecting the vermis (summary by Synofzik et al., 2011 ).Heterozygous mutation in the ITPR1 gene can also cause SCA29 ( OMIM[mendelian.co] vermis atrophy Dysmetria Peripheral neuropathy Progressive Cerebellar hypoplasia Broad-based gait Scanning speech Generalized myoclonic seizures Kinetic tremor Sensory neuropathy[mendelian.co] Learn more Other less relevant matches: High match SPINOCEREBELLAR ATAXIA 15; SCA15 SCA15 is an autosomal dominant, adult-onset, very slowly progressive form of cerebellar[mendelian.co]

  • Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome

    Cranial computed tomography (CT) showed diffuse white matter low density and cerebellar vermis atrophy.[ncbi.nlm.nih.gov]

  • Hypogonadotropic Hypogonadism

    A substantial fraction of BNS cases may present with relatively selective atrophy of the superior and dorsal parts of the cerebellar vermis along with atrophy of the cerebellar[ncbi.nlm.nih.gov]

  • Minamata Disease

    The characteristic changes in the acquired cases were atrophy of the visual calcarine cortex and of the cerebellar vermis and/or hemisphere.[ncbi.nlm.nih.gov] CT revealed a bilateral, symmetric, low-density area in the visual cortex and diffuse atrophy of the cerebellar hemispheres and vermis, especially the inferior vermis.[ncbi.nlm.nih.gov] Marked atrophy of the calcarine cortex produced the sac-shaped low density areas between the occipital lobes and diffuse and marked cerebellar atrophy with enlargement of[ncbi.nlm.nih.gov]

  • Cerebellar Atrophy

    […] with tremor, cerebellar vermis atrophy, and optic-nerve thinning.[ncbi.nlm.nih.gov] We report the case of a young man who had been suffering for five years of progressive cerebellar syndrome. MRI showed marked cerebellar vermis atrophy.[ncbi.nlm.nih.gov] vermis atrophy with mild cerebellar hemisphere atrophy, associated with profound global developmental delay.[orpha.net]

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