Peripheral Polyneuropathy Flashcards

1
Q

3 categories of inherited polyneuropathies

A

Hereditary Motor and Sensory Neuropathy
Hereditary Sensory and Autonomic Neuropathy
Hereditary Motor Neuropathy

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2
Q

Most commonly inherited polyneuropathy

A

Hereditary motor and sensory neuropathy, AKA Charcot-Marie Tooth Disease

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3
Q

Recurrent short term episodes of motor and sensory mononeuropathies due to nerves being sensitive to pressure

A

Hereditary neuropathy with liability to pressure palsy (HNPP)

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4
Q

HMSN is similar to what else in terms of same gene mutation

A

HNPP (hereditary neuropathy with liability to pressure palsy)

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5
Q

Sensory loss along with thermal day’s regulation, bladder dysfunction and cognitive deficits

A

Hereditary sensory and autonomic neuropathy

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6
Q

Progressive weakness and atrophy of UE and LE

A

Hereditary motor neuropathy

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7
Q

Most common acquired polyneuropathy

A

Diabetes mellitus

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8
Q

Typical distribution of symptoms of acquired polyneuropathy

A

Symptoms are distal and progresses proximally

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9
Q

Multifocal motor neuropathy
Demyelination vs. axonal
Motor vs. sensory

A

Demyelinating

Motor

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10
Q

HMSN I, II, III, IV
Demyelination vs. axonal
Motor vs. sensory

A

I, III, IV = demyelinating, sensorimotor

II = axonal, motor > sensory

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11
Q

AIDP and CIDP
Demyelination vs. axonal
Motor vs. sensory

A
AIDP = Demyelinating or axonal, motor > sensory
CIDP = demyelinating, motor > sensory
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12
Q

Diabetic neuropathy
Demyelination vs. axonal
Motor vs. sensory

A

Demyelination and axonal loss

Sensorimotor

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13
Q

Lead toxicity
Demyelination vs. axonal
Motor vs. sensory

A

Axonal loss

Motor > sensory

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14
Q

B12 deficiency
Demyelination vs. axonal
Motor vs. sensory

A

Axonal loss

Sensorimotor

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15
Q

Friedrich’s ataxia
Demyelination vs. axonal
Motor vs. sensory

A

Axonal

Sensory

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16
Q

Gold toxicity
Demyelination vs. axonal
Motor vs. sensory

A

Axonal loss

Sensorimotor

17
Q

Classic triad of polyneuropathies

A
  1. Stocking/glove distribution
  2. Distal weakness
  3. Diminished/absent MSR
18
Q
Demyelinating vs axonal injury NCS:
Latency
CV
Amplitude
Temporal dispersion
A
Demyelinating = prolonged latency, decreased CV, Nml amplitude, increased temporal dispersion
Axonal = normal latency, normal CV, decrease amplitude, no temporal dispersion
19
Q
Demyelinating vs axonal injury EMG:
Fibrillations/PSWs
Myokymic discharges
Recruitment
Phases
A
Demyelinating = no fibs/PSWS, + myokymic discharges, decreased recruitment, normal phases.
Axonal = + fibs/PSWs, no myokymic discharges, decreased recruitment, polyphasic
20
Q

Hereditary vs acquired NCS:
Conduction block
CV
Temporal Dispersion

A
Hereditary = no conduction block, diffuse slowing CV, no dispersion.
Acquired = + Conduction block, focal slowing CV, increased dispersion.