section name header

Table 14.3

Anatomical Localization in Neurological Diagnosis

Anatomical structureAssociated clinical features
MeningesHeadache, neck stiffness, photophobia
Cerebrum
Seizure, dysphasia, hemianopia, neglect, apraxia, dyscalculia, other disturbances of higher cortical function
  • Subcortical
Bradyphrenia, executive dysfunction, personality change
  • Pyramidal
Pyramidal distribution weakness, hyper-reflexia, spasticity, extensor plantar
  • Extrapyramidal
Tremor, rigidity, bradykinesia, hemiballismus, chorea
  • Diffuse
Reduced conscious level, impaired attention
CerebellumNystagmus, dysarthria, dysmetria, ataxia, dysdiadokokinesis
Brainstem‘Crossed’ (e.g. ipislateral facial and contralateral limb weakness with a pontine lesion), other cranial nerve deficits +/- long tract signs, ‘locked-in’, quadriparesis
Spinal cordParaparesis or quadriparesis, sensory level (may be suspended, crossed and/or dissociated), extensor plantars, sphincter and autonomic dysfunction
Motor neurons/anterior hornMixed upper and lower motor neuron signs, fasciculations
Nerve rootsRadicular pain (deep within limb or radiating ‘electric shock’), weakness in a group of muscles, localized areflexia
Dorsal root gangliaAtaxia, pseudoathetosis, areflexia
PlexusPain then weakness > sensory disturbance, involves multiple root and nerve territories
Peripheral nerve
  • Mononeuropathy
Characteristic pattern of selective muscle weakness and sensory loss in a single limb
Weakness proportional to wasting (distal > proximal), glove and stocking sensory loss
  • Demyelinating
Proximal and distal weakness out of proportion to wasting, global areflexia
Pain, selective loss of pin-prick and temperature sensation, autonomic dysfunction, preserved power and reflexes
Neuromuscular junctionFatigable diplopia, ptosis, dysarthria, facial and proximal limb weakness, no sensory loss
MuscleCharacteristic distribution of weakness (often proximal), wasting, myalgia, no sensory loss