Symptoms of cerebellar ataxia
[DOC File]MOVEMENT DISORDERS AND ATAXIA
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From cerebellar (or rarely frontal) lesion. Akinetic-rigid gait: Stooped, shuffling, trouble starting and stopping, often with tremor, decreased arm swing, poor postural reflexes.
[DOC File]Cerebellum
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In humans, more marked is the unsteadiness of walking (gait ataxia) in patients with damage mainly affecting the anterior lobe vermis and intermediate zone. CEREBELLAR SYNDROMS Lesions involving large part of the cerebellum, including the neocerebellum results incoordination of …
[DOCX File]Viktor's Notes – Ataxias
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Early-Onset Cerebellar Ataxia With Retained Tendon Reflexes - as. Friedreich’s ataxia with retained tendon reflexes. ... less frequent symptoms - gaze palsy, slow saccades, decreased vibration sense, bladder dysfunction. rare symptoms - basal ganglia symptoms, dementia.
[DOCX File]Viktor's Notes – Cerebellar Disorders
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cerebellar artery (pica) - inferior hemispheres (up to primary fissure), inferior vermis, deep nuclei, inferior peduncle, lateral medulla oblongata, choroid plexus of 4th ventricle. Ipsilateral limb ataxia
[DOC File]THE CEREBELLUM - FUNCTION AND PATIENT …
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Lesions of the cerebellum give rise to (1) incoordination (ataxia) of volitional movement, (2) disorders of equilibrium and gait, (3) a tremor that derives from ataxia and hypotonia, and (4) a reduction in muscle tone.
[DOC File]Anatomy and Pathology of the Cerebellar Peduncle
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Lesions of the cerebellar peduncle result in variable clinical symptoms, ranging from vertigo or vomiting as the only clinical presentation to facial palsy, ataxia, nystagmus, diplopia, dysphagia, dysarthria, deafness, contralateral motor weakness, trigeminal sensory loss, dysmetria of the limb, loss of pain and temperature sense, Horner's syndrome, and "locked-in" syndrome (1,4,5).
[DOC File]Progressive Supranuclear Palsy Update
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Ataxia of Acute or Subacute Onset. Cerebellar ataxia with extremely acute onset has two main causes: cerebellar haemorrhage (usually associated with headache, vertigo, vomiting, altered consciousness, and neck stiffness), and cerebellar infarction (in which cerebellar signs are usually combined with signs of brain stem ischaemia, and the presentation may mimic that of haemorrhage).
[DOC File]Table S2 – Detailed list of 51 neuromuscular …
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Table S2 – Detailed list of 51 neuromuscular disorders (16 mapped and 28 with a cloned gene) characterized by neurological symptoms such as epilepsy, spastic paraplegia, ataxia, etc. Entries are listed in alphabetical order but those that have an OMIM number are indicated first, followed by those that have appeared only in PubMed publications. All entries indicated in red are allelic to the ...
[DOCX File][Date]
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Hereditary Ataxia is a group of genetic disorders characterized by slowly progressive incoordination of gait and often associated with poor coordination of hands, speech, and eye movements. Frequently, atrophy of the cerebellum occurs.
[DOC File]School of Medicine - LSU Health New Orleans
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Cerebellar ataxia - limb ataxia, gait imbalance Associated symptoms Anatomy & vascular territory +/- Lateropulsion, vertigo, nausea and vomiting, nystagmus, ocular tilt reaction, dysphonia and dysphagia, (nucleus ambiguous: IX, X, XI), ipsilateral facial thermalgesia (5th cranial nerve), Horner syndrome, contralateral thermalgesia of trunk and limbs (Wallenberg syndrome)
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