I don't think it matters whether or not this was ALS ( which I still think it is). But theres fasiculations and Weakness and atrophy those are LMNL signs. Theres sooo many sneaky questions in this exam, this isnt one of them.
Does anyone have any idea on this question? Thought it was ALS.
I was thrown off because I didn't realize lower motoneuron = lower motor neuron face palm
"LMN deficits... dysarthria, dysphagia, asymmetric limb weakness, fasciculations, atrophy
UMN deficits... pseudobulbar palsy (i.e. dysarthria, dysphagia, emotional lability, spastic gait, clonus])"
-- FA 2019 p.518
"The loss of lower motor neurons leads to weakness, twitching of muscle (fasciculation), and loss of muscle mass (muscle atrophy)".
https://www.medicinenet.com/script/main/art.asp?articlekey=33870
I figured since the answer was mis-spelled, it couldn't be the answer.
I treated this like Werdning Hoffman/SMA ("tongue fasciculations"), and just kind of accepted it being weird to be in a 55-year-old.
submitted by โtherealslimshady(42)
Here is my personal way how I reasoned to the correct answer, if it helps anyone. First off, I recognized she probably has ALS, as she has purely motor symptoms (no sensory symptoms) that include both UMN (3-week history of muscle cramps) and LMN lesions (fasciculations, atrophy). In ALS, you have damage to anything that is composed of UMNs and LMNs. UMNs are found in (A) cerebral white matter, (B) corticospinal tract, and (C) internal capsule. I picked (D) for two reasons: (1) she has more LMN symptoms than UMN symptoms (the only UMN symptom was muscle cramps), and (2) choices A, B, and C are all UMNs, and so they can't all be right.
That's just what was going on through my brain. Very convoluted I know and might have errors, but if I helped at least 1 person then I did my job.