Week 6 Flashcards

0
Q

2 types of declarative memory

A
  • episodic memory - recalls events

- semantic memory - recalls facts/information

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1
Q

Guideline for Dementia Eval

A
  • General cognitive Screen - MMSE
  • depression screen
  • structural imaging - rule out structural causes
  • labs: CBC, CMP, LFT, TSH, B12
  • special: RPR, FDG-PET, genetic testing
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2
Q

procedural memory
working memory
prospective memory

A

procedural memory: unconsciously learned skills
working memory: manipulation of information
prospective memory: remembering to remember

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3
Q

which lobe is being tested in the following assessments?
List learning (MMSE)
Copy (visual memory)
recall later (visual memory)

A
List learning (MMSE) - dominant medial temporal lobe
Copy (visual memory) - biparietal lobes
recall later (visual memory - non-dominant medial temporal lobe
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4
Q

Frontal lobe function tests

A

Preservation: mnmnmnmnmn
set shifting - Trails: 1 Sunday 2 Saturday….
response inhibition - Stroop: colored words
Phonemic Fluency: F-word in 60 secs quality vs quantity

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5
Q

Deferential Dx of Dementia

A

VITAMINS C D
vascular, infection, trauma, autoimmune, metabolic/toxic, inflammation, neoplastic, seizure, congenital/developmental (inherited), degenerative

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6
Q

What are the 2 components of Nystagmus

A

smooth pursuit
saccade

*nystagmus is described in terms of the direction of saccade

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7
Q

What are the accessory oculomotor nuclei and their functions

A

riMLF - integrator for vertical saccade
INC
PPRF - integrator for horizontal saccade
pretectal area

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8
Q

All the inputs to VNC

A

vestibular input:
crista (semicircular canals) terminate in S, MVN
maculae (sacculus and utriculus) terminate in LVN

spinovestibular input:
from all level of spinal cord - proprioreceptive input

cerebellar input:
vestibulocerebellum(floccular node) –> FN –> VNC –> VST
spinocerebellum (vermis) –> fastigial nucleus –> VNC–> ReSt, VST
from bilateral fastigial via juxarestiform body

accessary oculomotor input:
from visual cortical areas via accessary oculomotor nuclei

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9
Q

Cortical area that have voluntary saccade control

A

dorsolateral prefrontal cortex
FEF
posterior parietal cortex

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10
Q

Cortical area that can smooth tracking moving objects

A

temporal eye field

occipital cortex

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11
Q

voluntary saccade scheme

A

PPC, FEF –> superior colliculus –> PPRF –> VI –> III

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12
Q

vestibulo-thalamo-cortical tract

A

cortical perception of movement (3a, 2b)

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13
Q

peripheral vs central lesion on vestibular

A

peripheral lesion:
CN VIII, unilateral peripheral lesion: vertigo, nausea, unsteadiness ( fall towards the side of lesion, nystagmus opposite to lesion

central lesion:
VNC lesion, absent vertigo, Romberg (fall away from lesion), nystagmus towards lesion

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14
Q

Saturday night palsy

A
  • schwann cells are damaged in area of compression
  • AP can’t propagate across compression site: conduction block - neuropraxia!
  • requires several hours of compression
  • recover by local dismantling and rebuilding of myelin sheath
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15
Q

Wallerian degeneration

A
  • cell body swells & RNA synthesis increases
  • immediate failure of AP, but delayed loss of distal responsiveness
  • myelin degeneration and axonal atrophy in 5 days
  • axonotmesis/ neurotmesis
16
Q

aberrant reinnervation

A

some axons end at different destination than original during reinnervation of surviving axons

17
Q

How to fix denervation

A
  • regeneration of injured axon

- sprouting : reinnervation

18
Q

Neuropathy

A

dysfunction in motor, sensory or autonomic function alone

19
Q

Define radicle

A

radicle = dorsal and ventral roots + spinal nerve

20
Q

radiculopathy

A

nerve becomes compressed in the spinal foramen by

  • herniated nucleus pulposus (soft disc)
  • osteophyte (hard disc)
21
Q

Radiculopathy

A

Sx corresponds to myotome/ dermatome/ sclerotome of compressed nerve

22
Q

2 types of plexopathy

A
  • brachial
  • lumbosacral
  • pattern of involvement in a limb > individual nerve/root lesion
23
Q

Mononeuropathy

A

abnormality of individual peripheral nerve

  • can be compression/ trauma
  • e.g. bell’s palsy, carpal tunnel syndrome, cubital syndrome….
24
Q

Polyneuropathy

A
  • bilateral, symmetric pattern
  • do not correspond to a single nerve/root
  • **distal segments involved initially –> move proximal if condition worsens
  • reduced/absent of muscle stretch reflex
  • metabolic/toxin/autoimmune/hereditary/idiopathic
25
Q

basic component of peripheral motor system

A

motor unit = neuron, axon, terminal branches, NMJs, muscle fibers

26
Q

CMAP vs MUAP

A

MUAP is the building block of recorded response

CMAP is the summation of MUAP - M wave

27
Q

patterns of abnormality of EMG on demyelinating vs axonal /motor neuron lesion

A

demyelinating: very slow conduction

axonal/ motor: mildly slow conduction

28
Q

parameters of voluntary motor unit potential (MUP) - summated activity of muscle fibers in one motor unit

A

size (amplitude & duration)
configuration
stability
firing rate (recruitment)

29
Q

2 abnormalities findings during rest activity in needle EMG

A
  • positive waves & fibrillation potentials - axon to muscle fiber is damaged
  • Fasciculation potential - can be normal/ abnormal
30
Q

MUP of early vs late reinnervation

A

early (2-6 months): polyphasic

late (1-2 years): large & rapid firing

31
Q

An estimate of heritability

A

H^2 = 2( C_mz - C_dz)

32
Q

Genes of MS

A

HLA - A
HLA DRB1
HLA DWB1
HLA DRA