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another name for vestibulocerebellum
archicerebellum, floccular node
another name for spinocerebellum
paleocerebellum, vermis
another name for neocerebellum
cerebrocerebellum, pontocerebellum
symptoms of vestibulocerebellar lesions
truncal ataxia, postural sway, nausea, impaired VOR, cerebellar nystagmus
symptoms of spinocerebellar lesions
hypotonia esp in prox mm, hypermetria, inability to decelerate, rebound phenomena, lack of motor plasticity, limb ataxia, wide BOS, fall randomly, intention tremor
symptoms of neocerebellar lesions
movt decomposition, asthenia, dysmetria, dysdiadokinesia, dysarthria, mm dysygnergy, ocular dysmetria
symptoms of sensory ataxia
no proprioception or vibratory sense, worse w/ EC, slapping foot gait
symptoms of vestibular ataxia
vertigo, nausea, no balance, nystagmus
symptoms of frontal ataxia
dementia, cognitive deficits
types of acquired ataxias
symmetrical & asymmetrical ataxias
causes of symmetrical ataxias
intoxifications, infections, Lyme disease, hypothyroidism, genetic disorders, high altitude cerebral oedema, hydrocephalus
causes of asymmetrical ataxias
stroke, TBI, infections, demyelination, tumours, trauma, AIDs, cervical spondylosis
types of inherited ataxias
fredereichs & spinocerebellar ataxias
most common hereditary ataxia
frederichs
pathogenesis of fredereichs
mutation in frataxin gene
dx of fredereichs
EMG, CSF, nerve conduction velocity, MRI, DNA, <25yrs
symptoms of fredereichs
progressive weakness, fatigue, dysarthria, dysphagia, dec sensation, hyporeflexia, spasticity, pes cavus, scoliosis
sequence of loss of sensation in fredereichs
1. vibration 2. proprioception 3. light touch 4. pain 5. temp
inheritance of spinocerebellar ataxia
autosomal dominant
dx of spinocerebellar ataxia
MRI, DNA, >18yrs
symptoms of spinocerebellar ataxia
ataxia, dementia, slow eye movts, visual loss, genetic anticipation
which inherited ataxia is more fatal?
spinocerebellar ataxia
inheritance of frederichs ataxia
autosomal recessive
causes of SCI
trauma, disease processes, vascular insult, degeneration, prolapsed IV disc, spina bifida, MS, ALS, transverse myelitis
tetraplegia
no motor &/or sensory function in arms, trunk, legs & pelvic organs due to damaged C/cord
paraplegia
no motor &/or sensory function in T/L/S spine- arm function okay, trunk/legs/pelvic organs possibly involved
neurological level
most caudal segment w/ intact sensation & G3 motor function
sensory level
most caudal segment w/ normal sensory function bilat
motor level
most caudal segment w/ G3 strength, provided the segment above has G5 bilat
skeletal level
level where by X-ray, the greatest vertebral damage is found
complete injury
absence of sensory & motor function below lesion level & in lowest sacral segment
incomplete injury
partial preservation of sensory &/or motor function below neuro level & incl lowest sacral segment
complete transverse syndrome
complete loss of motor power & sensation below injury level
central cord syndrome
loss of power & sensation in ULs w/ minimal loss in LLs
most common group affected by central cord syndrome
elderly
most common mechanism of central cord syndrome
hyperextension injury
anterior artery syndrome
loss of motor power, pain & temp w/ preservation of proprioception, vibration & touch
brown-sequard syndrome
loss voluntary motor control on same side of cord damage + loss of pain & temp on contralat side
onset of CES
20-29yrs, M
symptoms of CES
saddle anaesthesia, inc freq urination, inability to void, no sphincter control, motor & sensory loss in LLs, pain w/ altered posture
ASIA A
complete, no sensory/motor function preserved below neuro level + absent S4/S5
ASIA B
incomplete, sensory but no motor function preserved below neuro level + S4/S5 present
ASIA C
incomplete, motor function preserved below neuro level & more than 1/2 key mm below NL < G3
ASIA D
incomplete, motor function preserved below NL & at least 1/2 key mm below NL >= G3
ASIA E
normal sensory & motor function
ant spinal artery supplies how much of SC?
front 2/3
SCI most commonly caused by
traumatic causes
most common cause of CES
central lumbar disc herniation
3 most common cause of death in SCI
pnemonia/influenza, septicaemia, cancer
spinal shock
temporary loss of cord mediated reflexes/function below lesion level
80% of SCI present with ---
spasticity
why don't you use banding when testing sensation for SCI?
may create false +ves due to vibration
what % of WC users report shoulder pain?
70%
ANS controls
BP, HR, temp, appetite, fluid balance, bladder function, GI motility, carb & fat metabolism, sleep & sexual function
autonomic dysreflexia
exaggerated sympathetic response to noxious stimuli below lesion level, occurs in @ or above T6
causes of autonomic dysreflexia
bladder/renal, bowel, skin, #, infection, pain, sexual stimulation, onset of labour
symptoms of autonomic dysreflexia
severe headache, inc BP, red blotchy rash, anxiety, snuffly sensation, bradycardia
syringomyelia
cyst formation @ injury site
up to 1/3 of bone mass may be lost in first -- months post SCI
16
postural hypotension
blood pools in abdomen & LL
poikilothermia
lose ability to shiver/sweat w/ SCI above T6
when does heterotopic ossification most commonly occur
during first year post injury
causes of pressure injuries
unrelieved pressure, shearing, friction, trauma
dizziness affects --% of people >40yrs
40%
causes of dizziness
drug interactions, orthostatic hypotension, cardiac disorders, agoraphobia, VBI, cerebral pathology, migraine, Cspine pathology
symptoms of vestibular deficits
nausea, vertigo, visual impairment, gait/balance disorders, nystagmus
types of nystagmus
spontaneous, positional or evoked
VOR
acts to keep what we see stable
VSR
acts to stabilise the body
most common vestibular disorder
BPPV
pathogenesis of BPPV
otoconia from the utricle becomes dislodged
dx of BPPV
Hallpike-Dix
symptoms of UVH
nystagmus, oscillopsia, blurred vision, gait/balance impaired, vertigo
symptoms of BVH
oscillopsia, ataxia, postural disturbance, NO VERTIGO
irritative vertigo
over-active vestibular system caused by inflam of vestibular apparatus/nerve
ablative vertigo
under-active vestibular system caused by degeneration
Is MND more common in men or women?
M~3:2
peak onset MND
50-70yrs
what % of MND has familial form
5-10%
symptoms of MND if LMN predominates
mm atrophy in specific mm, hyporeflexia, dec or normal tone, fasciculations
symptoms of MND if UMN predominates
widespread mm wasting, hyperreflexia, hypertonia, primitive reflexes
dx of MND
clinical dx, EMG, excl other disorders
4 types of MND
ALS, PBP, PMA, PLS
early symptoms of MND
cramps, slowed movt, mm stiffness, emotional responses triggered easily, dysarthria, dysphagia
what is NOT affected in MND
sensory or cognitive function
symptoms of advanced MND
depression, weight loss, malnutrition, venous thrombosis, contractures, RF
what type of MND has mixed bulbar & limb signs, + is more common in older F
PBP
most common neurological disease affecting young AUS
MS
MS is more prevalent
further from the equator
peak onset of MS
20-25yrs
Is MS more common in men or women?
F~3:1
sites of MS plaques
close relationship to veins, periventricular regions, cerebellar white matter, optic nerves, BS, SC
which MS clinical course makes up 85% of presentations?
relapsing-remitting
dx of MS
at least 2 episodes of symptoms, diffuse CNS areas involved, neurophysiological, radiological testing, lumbar puncture, blood tests
initial symptoms of MS
motor, sensory, pain, optic, cerebellar ataxia, bladder/bowel dysfunction, Lhermitte's sign
Lhermitte's sign
electric shock sensation w/ passive neck flexion
later symptoms of MS
motor impaired +/- fatigue, sensory deficit, ataxia, sphincter & sexual dysfunction, optic neuritis, diplopia, intention tremor, cognitive impairment
fatigue in MS is worse when?
hot weather, strenuous activity, immersion in hot water
which race is MS most common in?
Caucasians
--% of people aged >65yrs will fall in any given year
30%