NEURO 5 Flashcards
chronic hereditary sensory motor neuropathy
CMT1a commonest
acute autonomic neuropathy
GBS, popyphyria
chronic autonomic neuropathy
DM, amyloidosis, heriditary
MND is what
what in summary symptoms do px get
neurodgen condition, loss of motor neurones from cortex of brain
U/LMN signs without sensory symptoms
MND extremities which is more common
Upper > lower
what other forms of MND
bulbar - worst prognosis
thoracic
UMN
LMN
bulbar symptoms
what is generalised into
who
chewing, talking, swallowing. Cranial nerves 9-12
generalised into ALS
F>M, 60-80yo
ALS symptoms
genetics
ix
rx
LMN in arms - weak flexors. UMN in legs - weak extensors
idiopathic. familial - gene on chromosome 21
absence of sensory symp. EMG. neuroimaging - rule out
Riluzole
split hand syndrome
ALS
PLS
UMN signs only
PMA
LMN signs only affects distal muscles before proximal ones
best and worst prognosis in MND
best is PMA
worst is bulbar
cord transection cervical
T/L/S
quadraplegia
paraplegia
cord compressione BSS
ipsilateral motor and dorsal column loss
contralateral spinothalamic loss
central cord syndrome how and what r the symp
hyperflexion to already steotatic neck
UL weakness - distal cape like spinothalamic sensory loss
LL power and DC preserved