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875 Possible Causes for Diffuse Osseous Demineralization, Dysmetria

  • Lyme Neuroborreliosis

    We report the case of a 23-year-old male patient who suddenly developed right hemiparesis, cerebellar ataxia, dysarthria, and bilateral dysmetria.[] osseous structures.[] The neurological examination showed a Horner syndrome and dysmetria on the right side, dysarthria, as well as gait ataxia.[]

  • Lyme Disease

    osseous structures.[] The one patient in the doxycycline group who reported severe arthralgia at the last follow-up had a history of multiple dorsal and lumbar fractures with diffusely demineralized[]

  • Cerebellar Stroke

    Andreason suggests the presence of cognitive dysmetria due to cerebellar involvement in schizophrenia which is analogous to motor dysmetria so far described in cerebellar[] Dysmetria and ataxia were most resistant to rehabilitation.[] Dysfunctional cortico-cerebellar circuits cause 'cognitive dysmetria' in schizophrenia. Neuroreport 1998;9:1895-9. 5. Starkstein SE, Boston JD, Robinson RG.[]

    Missing: Diffuse Osseous Demineralization
  • Intracerebral Hematoma

    After the spontaneous relief of initial symptoms by traumatic carotid-cavernous fistula (CCF), paradoxical worsening of patient's condition can be followed. We present a case of a 60-yr-old man whose audible bruit from a traumatic CCF had completely disappeared. A few days later, however, the patient had[…][]

    Missing: Diffuse Osseous Demineralization
  • Cerebellar Neoplasm

    Tumors of the cerebellum Supplemental material : Video of saccadic dysmetria (same patient as above).[] Lesions involving the cerebellar hemispheres are more likely to show limb ataxias and associated dysmetria.[] […] quadrantanopia, behavioral alterations Occipital lobe Contralateral hemianopia Thalamus Contralateral sensory loss, behavioral changes, language disorder Cerebellum Ataxia, dysmetria[]

    Missing: Diffuse Osseous Demineralization
  • Niemann-Pick Disease Type C

    We clinically evaluated patients' neurological involvement, giving a score of severity ranging from 0 (best) to 3 (worst) for gait abnormalities, dystonia, dysmetria, dysarthria[] Neurological examination revealed a broad-based ataxic gait, limb dysmetria, downward vertical gaze palsy, brisk lower limb reflexes and ankle clonus, while neuropsychological[] Typical neurological manifestations include vertical supranuclear gaze palsy, saccadic eye movement abnormalities, cerebellar ataxia, dystonia, dysmetria, dysphagia and dysarthria[]

    Missing: Diffuse Osseous Demineralization
  • Multiple Sclerosis

    Neoplasms and reactivation of latent viruses have been observed in individuals taking fingolimod. Merkel cell carcinoma (MCC), a rare neuroendocrine skin cancer, is associated with immunosuppression and can be triggered by the oncogenic Merkel cell polyoma virus (MCPyV). We report a case of a 61-year-old man with[…][]

    Missing: Diffuse Osseous Demineralization
  • Autosomal Recessive Spinocerebellar Ataxia 8

    They may also have difficulty with movements that involve judging distance or scale (dysmetria).[] […] begin in adulthood 0003581 Autosomal recessive inheritance 0000007 Cerebellar atrophy Degeneration of cerebellum 0001272 Dysarthria Difficulty articulating speech 0001260 Dysmetria[] They may also have difficulty with movements that involve judging distance or scale ( dysmetria ).[]

    Missing: Diffuse Osseous Demineralization
  • Spinocerebellar Ataxia Type 12

    Abstract SCA12 is an autosomal dominant cerebellar ataxia characterized by onset in the fourth decade of life with action tremor of arms and head, mild ataxia, dysmetria,[] […] is a progressive autosomal-dominant disorder, caused by a CAG/CTG repeat expansion in PPP2R2B on chromosome 5q32, and characterized by tremor, gait ataxia, hyperreflexia, dysmetria[] […] consent has been received Technical Information Clinical Significance: Detect repeat expansions in SCA12 gene Typical Presentation: Tremor of arms and head, mild ataxia, dysmetria[]

    Missing: Diffuse Osseous Demineralization
  • Adult-Onset Autosomal Recessive Cerebellar Ataxia

    They may also have difficulty with movements that involve judging distance or scale ( dysmetria ).[] Gait ataxia, dysarthria, dysmetria, nystagmus, muscle wasting and dystonia are seen in the late stages of the disease.[] A slowly progressive cerebellar syndrome with various combinations of oculomotor disorders, dysarthria, dysmetria/kinetic tremor, and ataxic gait are key presenting features[]

    Missing: Diffuse Osseous Demineralization

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