Neurology Flashcards
Non-dominant parietal lesion - clinical signs
Inattention
Neglect
Impaired constructional ability
Dominant parietal lobe lesion - clinical signs
Gerstmann's syndrome: Finger agnosia Agraphia Acalculia Right-left disorientation
Gerstmann’s syndrome
Finger agnosia
Agraphia
Acalculia
Right-left disorientation
- Due to dominant parietal lobe lesion (eg. left PCA stroke)
Common peroneal neuropathy
Inability to heel walk Foot drop Weakness - foot eversion (not inversion, due to intact posterior tibial), dorsiflexion Sensory - lateral aspect dorsum foot Reflex - intact
L5 radiculopathy
Inability to heel walk Foot drop (foot dorsiflexion) Weakness - foot inversion and eversion, knee flexion Sensory - dorsum foot Reflex - hamstring loss, ankle intact
S1 radiculopathy
Inability to toe walk
Weakness - plantar foot extension, hip extension, knee flexion, toe flexion
Sensory - plantar/lateral foot
Reflex - ankle jerk loss
Internuclear opthalmoplegia (INO)
Injury to medial longitudinal fasciculus (MLF) within the dorsomedial pontine or midbrain tegmentum.
Symptoms:
Ipsilateral adduction weakness
Contralateral nystagmus
Normal convergence
Anton’s syndrome
Denial of blindness
- Due to bilateral posterior cerebral artery infarction
Causes of deep intracerebral haemorrhage (eg. putamen, thalamus, brainstem, cerebellum)
Hypertension
Rupture of deep penetrating arteries
Causes of lobar intracerebral haemorrhage (eg. cortex, subcortical white matter)
Amyloid angiopathy
Tumour
Arteriovenous malformation
Aneurysm
Most common Guillain-Barre syndrome (GBS) precipitating infections
Campylobacter jejuni gastroenteritis HIV Influenza-like illness CMV EBV Mycoplasma pneumoniae
Guillain-Barre syndrome - diagnosis
CSF - albumino-cytologic dissociation (high protein, normal white cell count)
NCS - prolonged/absent F-waves, proximal block (distal conduction velocities normal)
GM-1 - 40-50% GBS
GQ1b - in Miller Fisher variant
Progressive supranuclear palsy (PSP) - presentation
Parkinson’s plus syndrome
Gait disturbance
Falls
Opthalmoplegia - occurs late (3-5 years)
Lewy Body dementia (LBD) - presentation
Parkinson’s plus syndrome
Visual hallucinations
Fluctuating cognition
Parkinsonism
Corticospinal degeneration (CSD) - presentation
Parkinson's plus syndrome Progressive asymmetric movement disorder (affects 1 limb initially) Akinesia Rigidity Focal myoclonus Alien limb phenomena