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827 Possible Causes for Truncal Ataxia

  • Opsoclonus-Myoclonus Syndrome

    Opsoclonus, myoclonus, and truncal ataxia were noted.[] A 69 year-old man developed sudden-onset multidirectional, constant, involuntary ocular movements associated with vertigo, truncal ataxia and involuntary movements of the[] Opsoclonus when accompanied by other symptoms of central nervous system involvement (head, appendicular myoclonus and truncal ataxia) constitutes a clinical picture, known[]

  • Cerebellar Ataxia

    , hypotonia and cerebellar dysfunction (nystagmus, ataxic gait, truncal ataxia, dysarthric speech and intention tremor), associated with cerebellar hypoplasia.[] Key points • The peak incidence of acute cerebellar ataxia is in children between 2 and 4 years old, most commonly presenting as truncal, rather than extremity, ataxia. •[] Typical clinical signs and symptoms of autosomal dominant ataxias (ADCA) include the following: Limb and truncal ataxia Hyperreflexia and spasticity (pyramidal signs) are[]

  • Spinocerebellar Ataxia Type 1

    Neurological examination 5 years after onset revealed slow eye movement with nystagmus as well as limb and truncal ataxia.[] They may fall to the side of the lesion NOTE: patients with disease of the vermis and flocculonodular lobe will be unable to stand at all as they will have truncal ataxia–they[] ataxia Instability or lack of coordination of central trunk muscles 0002078 Urinary bladder sphincter dysfunction 0002839 Showing of 65 Last updated: 6/1/2019 Making a diagnosis[]

  • Olivopontocerebellar Atrophy

    A patient with olivopontocerebellar atrophy presented with an asymmetric parkinsonian syndrome consisting of right limb rigidity, bradykinesia, masked facies, and a hypophonic, monotonous voice. Right limb clumsiness suggested corticospinal tract involvement. Gait was slightly wide based, but no other cerebellar or[…][]

  • Dandy-Walker Syndrome

    ataxia Instability or lack of coordination of central trunk muscles 0002078 Showing of 19 Last updated: 1/1/2020 In most cases, the exact cause of Dandy-Walker complex is[] […] vermis 0002951 Posterior fossa cyst at the fourth ventricle 0000933 Sporadic No previous family history 0003745 Thinning and bulging of the posterior fossa bones 0000931 Truncal[]

  • Friedreich Ataxia

    The clinical picture consisted of progressive spastic gait, truncal and limb ataxia, dysarthria, nystagmus, hyperreflexia with knee and ankle clonus and extensor plantar response[] Ataxia (truncal and limb), lower extremity weakness, and sensory loss is progressive and gradually extends from distal to proximal [6] [8].[] ataxia and Stomping gait) Vision impairment Hearing impairment Slurred speech[3] Abnormal curvature of the spine Dorsal column: Loss of vibratory sensation and proprioceptive[]

  • Acute Cerebellar Ataxia

    This patient developed symptoms of ACA, including nausea, vertigo, severe limb and truncal ataxia, and bilateral spontaneous continuous horizontal nystagmus with irregular[] In addition to his marked truncal ataxia and wide-based, staggering gait, he had slowness of speech, which is not commonly reported with this condition in the literature.[] Abstract Acute Cerebellar Ataxia (ACA) is not infrequent disorder in childhood characterized by sudden onset of such cerebellar signs as truncal ataxia, dysmetria, tremors[]

  • Subacute Sclerosing Panencephalitis

    He had varicella-like illness with vesicular, itchy truncal rash erupting one month prior to the onset of these symptoms.[] A 5-year-old boy presented with acute-onset cerebellar ataxia without associated encephalopathy, focal motor deficits, seizures or cognitive decline.[]

  • Primary Torsion Dystonia

    Abstract A GAG deletion in the DYT1 gene accounts for most early, limb onset primary torsion dystonia (PTD). The genetic bases for the more common adult onset and focal PTD are less well delineated. Genetic loci for an "intermediate dystonia" phenotype and for torticollis, named DYT6 and DYT7 respectively, have[…][]

  • Alcoholic Cerebellar Degeneration

    ataxia Unsteady gait Nystagmus May be clinically asymptomatic in some individuals Laboratory No specific laboratory abnormalities Radiology description Atrophy of the anterior[] Midline lesions can produce severe gait and truncal ataxia.[] A 41 yo female with slow progressive ataxia, slurred speech since last 15 years. Truncal ataxia on neurological examination.[]

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