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1,053 Possible Causes for Ataxia, Hyperreflexia

  • Stroke

    The first patient (female, 50 years old) had dysarthria, nystagmus and trunk ataxia on admission. Her blood alcohol level was 2.3‰.[] An examination showed decreased strength on the right side, with hyperreflexia and an up-going plantar response.[] Dysarthria and right-sided limb ataxia were newly developed before DWI (after p-CTA).[]

  • Primary Progressive Multiple Sclerosis

    Spastic paraparesis and progressive ataxia are principal symptoms in this subset of patients.[] Affected individuals may have tremors, muscle stiffness (spasticity), exaggerated reflexes (hyperreflexia), weakness or partial paralysis of the muscles of the limbs, difficulty[] Abstract HDLS (Hereditary Diffuse Leukodystrophy with Spheroids) is a hereditary leukodystrophy whose main clinical manifestations include parkinsonism, spasticity, and ataxia[]

  • Pernicious Anemia

    The outcome was rapidly marked by febrile pancytopenia and ataxia leading to the diagnosis of pernicious anemia.[] […] impaired ability to coordinate movement (ataxia), a positive Babinski sign (outward motion of the big toe caused by stroking the sole of the foot), and/or exaggerated reflexes (hyperreflexia[] We report the case of a 60-year-old woman with a history of ataxia who sought evaluation after a syncopal episode.[]

  • Leigh's Disease

    Neurologic features include hypotonia, spasticity, movement disorders (including chorea), cerebellar ataxia, and peripheral neuropathy.[] A 4 1/2-month-old girl suffered from psychomotor retardation, generalized hypotonia, poor feeding, hyperreflexia, nystagmus, optical atrophy and choreoathetosis from the age[] The second attack was noted one month later, to be associated with hypotonia and truncal ataxia.[]

  • Amyotrophic Lateral Sclerosis

    Blood from ND patients with PD, ALS and Ataxia with movement dysfunctions were obtained to analyse mRNA and protein expressions of the above mentioned factors in lymphocytes[] […] remains normal Physical exam neck ptosis (neck drop) due to neck extensor weakness manual muscle testing elicits muscle cramping upper motor neuron (UMN) signs spasticity hyperreflexia[] A 75-year-old female patient presented with cerebellar ataxia, bulbar palsy and cognitive impairment.[]

  • Vertebrobasilar Insufficiency

    Examination revealed a right third nerve palsy and ataxia. Symptoms and signs resolved over 24 hours.[] Their symptoms included vertigo, dysarthria, dysphagia, syncope, motor and/or sensory disturbance, and cerebellar ataxia. Six had multiple stenotic lesions.[] CANVAS Syndrome CANVAS is an easy to remember acronym for cerebellar ataxia, neuropathy, and vestibular areflexia.[]

  • Friedreich Ataxia

    ataxia with retained reflexes.[] We report two patients with delayed-onset, hyperreflexia and gradually progressive disease.[] His examination was significant for spastic gait, hyperreflexia, and sensory neuropathy. Genetic testing revealed a compound heterozygous mutation in the FXN gene.[]

  • Multiple Sclerosis

    ‘Medusa head ataxia’: The expanding spectrum of Purkinje cell antibodies in autoimmune cerebellar ataxia.[] Abstract Based on one patient's enthusiastic report, eight patients with multiple sclerosis, seriously disabled with tremor and ataxia, were given oral tetrahydrocannabinol[] An 80-year-old man developed dysarthria, quadriplegia, sensory disturbance and ataxia in all limbs.[]

  • Behr Syndrome

    Keywords: Tremor; cerebellar ataxia; Behr syndrome; deep brain stimulation; ventral intermediate thalamic nucleus.[] […] loss and sensorineural hearing loss in childhood with variable presentation of other clinical manifestations including progressive external ophthalmoplegia, muscle cramps, hyperreflexia[] Onset : Early childhood Progression: Chronic progressive Clinical: Cerebellar ataxia plus syndrome / Optic Atrophy Plus Syndrome Ocular: Optic atrophy, nystagmus, scotoma,[]

  • Globoid Cell Leukodystrophy

    […] preserved intellectual and communicative capacity, in contrast to visual failure and severe central pyramidal and extrapyramidal motor disability with spasticity, dystonia, ataxia[] Hyperreflexia. Clonus. Pyramidal paresis of limb or limbs. Extensor plantar responses. Unsteadiness of gait. Psychomotor retardation. Dysphagia. Deafness.[] Late-onset krabbe disease (lokd) has first symptoms at ages 5 to 10 years, consisting of focal neurological signs, hemiparesis, cerebellar ataxia, cortical blindness, and[]

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