Exam 4 ALS Flashcards
Amyotropic Lateral Sclerosis is?
Idiopathic dz of UMN and LMN
NO sensation ∆s
ALS presentation?
Painless, progressive
BOTH upper and lowerMN signs in same limb
(spastic, hyperreflex, twitching, wasting)
TONGUE fasiculations
Weakness starts in hands/arms then legs
ALS diagnostics?
NCS findings?
EMG findings?
Imaging findings?
Clinical
NCS = N
EMG = widespread involv of prox and distal mm
Imag = N
ALS prognosis?
Time b/w sxs and death = 27 - 43 months
UMN lesion presentation?
Dependent on level of lesion
Spasticity (Initial resistance that gives way)
Hypertonia (Limbs held in position of strongest mm contraction)
Hyper-reflex
Clonus
Babinski
Abdominal stroke reflex absent
LMN lesion presentation?
Hyporeflex
Hypotonia
Fasciculation
Wasting