Neurology Flashcards
Name some features of parietal lobe lesions
sensory inattention
apraxias
astereognosis (tactile agnosia)
inferior homonymous quadrantanopia
Gerstmann’s syndrome (lesion of dominant parietal): alexia, acalculia, finger agnosia and right-left disorientation
Name some features of occipital lobe lesions
homonymous hemianopia (with macula sparing)
cortical blindness
visual agnosia
Name some features of temporal lobe lesions
Wernicke’s aphasia: this area ‘forms’ the speech before ‘sending it’ to Brocas area. Lesions result in word substituion, neologisms but speech remains fluent
superior homonymous quadrantanopia
auditory agnosia
prosopagnosia (difficulty recognising faces)
Name some features of frontal lobe lesions
expressive (Broca’s) aphasia: located on the posterior aspect of the frontal lobe, in the inferior frontal gyrus. Speech is non-fluent, laboured, and halting
disinhibition
perseveration
anosmia
inability to generate a list
What is Friederich’s ataxia caused by?
Friedreich’s ataxia is the most common of the early-onset hereditary ataxias. It is an autosomal recessive, trinucleotide repeat disorder characterised by a GAA repeat in the X25 gene on chromosome 9 (frataxin).
Name some neurological features of FA
absent ankle jerks/extensor plantars
cerebellar ataxia
optic atrophy
spinocerebellar tract degeneration
Name some other features of FA
hypertrophic obstructive cardiomyopathy (90%, most common cause of death)
diabetes mellitus (10-20%)
high-arched palate
Name some features of Horner’s syndrome
Miosis
Anhidrosis
Ptosis
Enophthalmos
Name some central causes of Horner’s
MS
Syringomyelia
Stroke
Encephalitis
Tumour
Name some preganglionic causes of Horner’s
Pancoast’s tumour
Thyroidectomy
Trauma
Cervical rib
Name some postganglionic causes of Horner’s
Carotid artery dissection
Carotid aneurysm
Cavernous sinus thrombosis
Cluster headache
What is Froin’s syndrome?
describes an increase in CSF protein below a spinal canal blockage (e.g. tumour, disc, infection)
How many days after acute stroke should anticoagulation be commenced?
14 days
Name some features of CJD
dementia (rapid onset)
myoclonus