Ataxia and gait disturbance

Introduction

  • Ataxia often erroneously considered due to cerebellar dysfunction
  • Isolated lesions of cerebellum are not the most common cause
  • Ataxia divided into motor and sensory
  • Can divide into systemic and primary CNS lesions

Differential

  • Systemic
    • Intoxication with diminished alertness – Ethanol, sedatives
    • Intoxications with preserved alertness – Phenytoin, carbamazepine, valproic acid, heavy metal intoxication
    • Other metabolic disorders – Hyponatraemia, inborn errors of metabolism, Wernicke’s

Differential

  • Disorders of nervous system
    • Cerebellar – Haemorrhage, tumor, infarction, degeneration, abscess
    • Cortex – Frontal tumor/haemorrhage/trauma, hydrocephalus
    • Subcortical – Thalamic infarction/haemorrhage, Parkinson’s, normal pressure hydrocephalus
    • Spinal cord – Spinal cord compression, posterior column disease
    • Peripheral neuropathy
    • Vestibulopathy

Motor ataxias

  • Aka cerebellar ataxias
  • Lateral cerebellar lesions lead to ipsilateral limb signs
  • Midline cerebellar lesions lead to axial incoordination
  • Supratentorial lesions
    • Small, deep infarctions
    • Lacunae of posterior limb of internal capsule
  • Thalamic nuclei infarction or haemorrhage can also produce motor ataxia with hemisensory loss
  • Frontal lobe lesions can cause contralateral motor ataxia through poorly understood mechanisms
  • Spinal cord compression can also present with motor ataxia

Sensory ataxias

  • Can be due to peripheral nerve, dorsal column or cerebellar input tract dysfunction
  • Can be compensated for by visual sensory inputs
  • Closed eye testing often exacerbates the issue

Gait disorders

  • Cerebellar/motor ataxic gait
    • Wide-based, unsteady irregular steps
  • Sensory ataxia
    • Abrupt movement of legs and slapping impact of feet
  • Apraxic gait
    • Ignition failure due to right or non-dominant hemispheric lesions
    • Frontal lobe dysfunction and normal pressure hydrocephalus can also lead to this
  • Festinating gait
    • Narrow based, miniature shuffling steps in Parkinson’s

Gait disorders

  • Circumduction gait
    • Outward swinging leg due to mild hemiparesis reflecting weakness of proximal lower extremity muscles
  • Waddling gait
    • Due to bilateral weakness of trunk and pelvic girdle muscles
  • Functional gait disorder
    • All testing normal but bizarre gait often resembling tightrope walking and threatening to fall but not
    • Dramatic functional gaits without falling actually demonstrate strength, balance and coordination are intact

Clinical features

  • Hx
    • Duration of onset
    • Fever
    • Headache
    • FHx of ataxia
    • Review of medications
    • Associated symptoms
  • Examination
    • Full neuro including cognition/alertness
    • Orthostatic vital signs
      • In the elderly, fluid replacement often corrects any unsteadiness
    • Gait testing
    • Cerebellar testing

Examination

  • Gait testing
    • Sitting
    • Standing, walk, turn and walk back
    • Heel walking and toe walking
  • Cerebellar vs. posterior column disease
    • Finger-nose testing: Testing with eyes closed identifies proprioceptive failure
    • Heel-shin testing:
      • Cerebellar: Heel may overshoot knee and then series of jerky movements
      • Posterior column: Difficulty locating the knee, heel weaves down shin or falls off

Examination

  • Rombergs
    • Stand with eyes open and arms outstretched
    • Inability to maintain standing posture (or sitting in extreme cases) confirms ataxia but not what type
    • Then close eyes, eliminating visual postural cues
    • If ataxia worsens, then Romberg’s positive = sensory ataxia with problem of proprioceptive input e.g. posterior columns. vestibular disease or peripheral neuropathy
    • If no change (negative), suggests motor ataxia

Examination

  • Tabes dorsalis (neurosyphilis)
    • Presents with wide-based slow gait staring at ground and cannot walk in darkness or with eyes closed
    • Due to loss of posterior column lower limb input
  • B12 deficiency
    • Also causes posterior column dysfunction
    • Initial unsteady gait can progress to weakness, ataxia and spasticity
  • Sensory examination
    • Always include proprioceptive testing sensation to pinprick
  • Nystagmus
    • Suggests process is intracranial vs. spinal cord or peripheral nervous system
    • Non-specific for actual cause

Geriatric patients

  • Gait becomes slowed, shortened stride and widened base with age
  • = Guarded gait
  • Seen in 25% of elderly patients
  • Also seen in Parkinson’s or normal pressure hydrocephalus

Last Updated on October 28, 2020 by Andrew Crofton