Chapter 8: Ataxia and Gait Disorders Flashcards
Which part of neuraxis causes ataxia
Cerebellar or sensory ataxia
Vermis vs. Hemispheric Cerebellar lesions
Vermal lesions: truncal and gait ataxia
Hemispheric lesions: Ipsilateral limb ataxia
Cerebellar Hemorrhage/Infarction
Abrupt onset of vertigo, vomiting, and inability to walk.
Level of arousal may be depressed if their is compression of fourth ventricle with hydrocephalus
Need neurosurgical decompression
Alcoholic Cerebellar Degeneration
Damages the vermis (truncal and gait ataxia)
Most common cause of acquired cerebellar degeneration.
Accompanied commonly by alcoholic polyneuropathy
Postinfectious Cerebellitis
Children age 2-7
Follows VZV or other virus
Limb, gait ataxia and dysarthria
Complete recovery
Paraneoplastic Cerebellar Degeneration
Pancerebellar syndrome: Truncal, gait, and limb ataxia; dysarthria; ocular motility issues (ocular dysmetria, nystagmus)
Acute/Subacute and then stabilizes with profound disability
Associated with Gynecologic or small cell lung cancer
CSF: elevated protein or lymphocytic pleocytosis
Anti-Yo, anti-Hu antibodies
Friedreich Ataxia
Aut. rec.
Progressive ataxia arms>legs, severe dysarthria
Childhood onset
Loss of reflexes, spasticity and extensor plantar responses, impaired vibration and position sense
Intention tremor
Rhythmic side-to-side oscillations of the limb as it approaches the target
Dysdiadochokinesia
Abnormality of rapid alternating movement (RAM)
Gait ataxia
Broad-based and unsteady
Dysarthria
Slow scanning and monotonous speech
Scanning speech
Pausing in between syllables of words, putting unusual emphasis or force on syllables
Drugs that cause ataxia
Phenytoin, barbiturates, antineoplastic agets
Inherited Episodic Ataxia
Brief episodes of ataxia, vertigo, nausea, and vomiting
Autosomal Dominant Spinocerebellar Degenerations
Cerebellar ataxia with or without additional neurologic signs.
Insidious onset