Physical Exam Findings in Cerebellar Ataxia
Cerebellar ataxia presents with characteristic physical examination findings that include widened-based gait, dysmetria, dysdiadochokinesia, truncal instability, dysarthria, and nystagmus—all of which persist regardless of visual input, distinguishing it from sensory ataxia. 1, 2, 3
Core Motor Examination Findings
Gait Abnormalities
- Widened base with unsteadiness and irregularity of steps is the cardinal feature of cerebellar ataxic gait 3
- Lateral veering during ambulation is characteristic 3
- Reduced step frequency with prolonged stance and double limb support duration 3
- High variability in all gait measurements distinguishes cerebellar from other gait disorders 3
- Truncal ataxia (difficulty maintaining posture) is particularly prominent with cerebellar vermian pathology 1, 2, 4
Limb Coordination Testing
- Dysmetria manifests as overshooting or undershooting during finger-to-nose and heel-to-shin testing 1, 5
- Dysdiadochokinesia (impaired rapid alternating movements) is evident during hand pronation-supination testing 3, 5
- Intention tremor appears during goal-directed movements 5
- Dyssynergia (loss of coordinated multi-joint movements) 1
Muscle Tone and Reflexes
- Antagonist hypotonia is typically present on examination 3
- Deep tendon reflexes may be normal or pendular 3
Oculomotor Examination Findings
- Nystagmus is a common finding, particularly cerebellar or central vestibular nystagmus 6, 5
- Ocular dysmetria (saccadic overshooting) 1
- Abnormal saccades and vestibulo-ocular reflex (VOR) are particularly helpful for differential diagnosis 7
- Ophthalmoplegia may be present in specific syndromes like Miller Fisher syndrome 1, 4
Speech and Swallowing Findings
- Dysarthria with scanning or ataxic speech pattern 1, 6, 5
- Dysphagic problems commonly emerge as disease progresses, particularly with thin consistencies 8
Critical Distinguishing Features
Romberg Test Interpretation
- Unsteadiness does NOT significantly worsen with eye closure in cerebellar ataxia, which is the key distinguishing feature from sensory ataxia 1, 2, 4
- The Romberg test cannot be properly performed in pure cerebellar ataxia as unsteadiness is present regardless of visual input 2
- Positive Romberg test (worsening with eyes closed) suggests sensory ataxia involving dorsal columns rather than cerebellar pathology 1
Associated Findings to Assess
- Pupillary abnormalities may suggest drug/toxin ingestion versus third cranial nerve compression 1
- Torticollis or resistance to head/neck motion may indicate craniocervical junction pathology, cord compression, or posterior fossa tumor 1
- Telangiectasias suggest ataxia-telangiectasia 1, 4
- Coexisting peripheral or central vestibulopathy symptoms can complicate the clinical picture 1, 2
- Brainstem involvement should be assessed as it commonly accompanies cerebellar pathology 2
Temporal Pattern Recognition
Acute/Subacute Presentation
- Headache with truncal ataxia and dysmetria suggests acute cerebellitis 1, 4
- Altered consciousness or additional neurological deficits in severe cases may indicate increased intracranial pressure or herniation 1
- Triad of ataxia, areflexia, and ophthalmoplegia is pathognomonic for Miller Fisher syndrome 1, 4
Chronic/Progressive Presentation
- Slowly progressive ataxia with hearing loss suggests superficial siderosis 1
- Progressive ataxia with cognitive and mood changes is common in degenerative cerebellar disorders 9
Common Pitfalls to Avoid
- Failing to distinguish cerebellar from sensory ataxia through proper Romberg testing leads to inappropriate diagnostic workup 8
- Mistaking weakness or hypotonia for ataxia in children requires careful examination 1
- Missing "pseudoataxia" from functional disorders which can mimic organic cerebellar disease 1
- Not recognizing that lurching gait triggered by head rotation indicates vestibular rather than cerebellar dysfunction 1
- Overlooking associated spinal cord signs (motor spasticity, sensory ataxia) that would warrant spine imaging in addition to brain imaging 1