Technical
Waveforms & Abnormalities
Clinical Diagnoses
Innervations
Miscellaneous
100

What type of nerve fibers does EDX evaluate?

What are Ia (large, myelinated) fibers?

100

What waveform abnormality would you expect to see with axonal loss?

What is a reduction in amplitude?

100

60yo M presents with weakness, dysphasia, and fasciculations. NCS SNAP and CMAP normal; EMG with abnormal activity, delayed recruitment, long duration large amplitude MUAP, and CRDs. What is the most likely diagnosis?

What is ALS?

ALS is a motor neuron disease; commonly affects males after the 6th decade. 

First signs: asymmetric atrophy, weakness, and fasciculations; dysphagia and dysarthria. Pseudobulbar signs: difficulty chewing, swallowing, and speech, along with unprovoked emotional outbursts. UMN and LMN signs.

Sensation is spared. 

100

What is the pure sensory nerve off the femoral nerve?

What is the saphenous nerve?

100

This term refers to the electrode known as "the green one" in nerve conduction studies.

What is the ground electrode?


Red electrode - Recording

Black - Reference

200

How do we define innervation ratio (IR)?

What is the amount of muscle fibers belonging to a single axon?

200

What is the common electrodiagnostic finding in GBS?

What is abnormal F waves?

200

Patient presents with difficulty making an "OK" sign as well as a fist. There are no sensation abnormalities. NCS with normal medial SNAP and normal median CMAP. EMG with abnormal activity to the FPL, normal APB. What is the diagnosis?

What is anterior interosseus syndrome (AIN) syndrome?

FPL and FDP weakness. 

EMG with abnormal findings in AIN muscles. NCS possible abnormal CMAP to the PQ. 

200

What is the origin of the nerve that innervates the lateral forearm?

What is the LAC, off the musculocutaneous nerve?

200

What is the timeframe for Wallerian degeneration for motor and sensory axons?

Distal motor axons - 7 days

Distal sensory axons - 11 days

300

What happens to amplitude and latency with a decrease in temperature?

Latency is prolonged

Amplitude is increased

300

In which condition will you see myokymic discharges?

What is radiation plexopathy?

300

40yo F presents with proximal fatigue and weakness, primarily in lower limbs, worse with rest but improved with exercise. 

NCS with normal SNAP, CMAP with low amplitude and incremental response with high-rate repetitive nerve stimulation. 

What is Lambert-Eaton syndrome?


300

What is the muscle innervated by the common fibular nerve?

What is the short head of biceps femoris?

300

This type of injury affects the axon of a nerve but not the supporting connective tissue that results in Wallerian degeneration?

a. Neurotmesis

b. Axonotmesis

c. Neuropraxia

What is axonotmesis?

Neurotmesis - complete transection

Axonotmesis - nerve crush injury

Neuropraxia - nerve compression injury

400

This term describes when the electrical impulse travels in the opposite direction of normal physiological conduction. 

What is antidromic?

400

In which conditions can you see early motor recruitment versus reduced recruitment?

Early recruitment - myopathic

Reduced recruitment - neuropathic 


400

Patient presents with proximal muscle weakness; started on a new medication a few weeks prior to presentation. NCS and EMG findings normal. What is the most likely diagnosis?

What is steroid myopathy?

Onset: weeks to years post use

Risk increased if on 30mg/day

EMG may be abnormal with small polyphasics in very severe cases

Treatment: stop steroid, rehab

400

This muscle is NOT dually innervated?

a. Flexor pollicis brevis

b. Gracilis

c. Biceps femoris

d. Lumbricals of the hand

What is the Gracilis?

FPB - Median and ulnar

Gracilis - Obturator

Biceps femoris - Short head (common fibular); Long head (Tibial branch of the sciatic)

400

Why are SNAPs normal in radiculopathy?

Lesions proximal to the DRG preserve the SNAP waveform despite clinical sensory abnormalities. 


Postganglionic injury results in Wallerian degeneration of both motor and sensory axons. There is physical separation of the axon from the cell bodies in the DRG and the ventral portion of the SC. CMAP and SNAP responses are diminished or absent.

500

What happens when the low frequency filter is raised?

Peak latency reduced

Amplitude is reduced


Reducing the high-frequency filter prolongs the peak latency and reduces the amplitude

500

A connection of the recurrent branch of the median nerve in the hand to the deep motor branch of the ulnar nerve producing an all ulnar innervated hand is known as what?

What is Riche-Canniue anastomosis?

500

Patient is a 50yo M with asymmetric weakness in his fingers, quadricep muscles, and foot drop that has been slowly progressing. Labs with increased CK. EMG with abnormal activity and early recruitment. 

What is inclusion body myositis? 

Asymmetric, slowly progressive, painless weakness in proximal and distal muscles. Patients often notice falling, tripping, and difficulty gripping objects as first symptoms. Atrophy present.

Affects adults 45-55 years, peaks at 70

Increased CK. Muscle biopsy with eosinophilic inclusion bodies and rimmed or cytoplasmic/basophilic vacuoles.

NCS: +/- abnormal SNAP and CAMP. 

EMG: abnormal activity, early recruitment, +/- short duration, small amplitude MUAP

No treatment. Not responsive to steroids.

500

What are the muscles innervated by the AIN?

FDP (digits II and III)

Flexor pollicus longus

Pronator quadratus

500

What are the expected conduction velocity variations by age?

CV for a newborn is 50% of that of an adult. AT 1 year, it is 80%. Equal to an adult by 3-5 years.

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