Neuro Flashcards

1
Q

Obtunded

A

dull & slow

will response appropriately

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2
Q

Stuporous

A

unresponsive to normal stimuli

aroused with strong stimuli

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3
Q

Comatose

A

Unconsciousness w/ no arousal

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4
Q

Head tilt vs head turn

A

Tilt
• Vestibular

Turn
• forebrain

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5
Q

Leaning

A

vestibular

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6
Q

Wide based stance

A

Vestibular

Cerebellar

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7
Q

De-cerebrate rigidity

A

Extension of all 4 legs + Opisthotonus
• Brainstem lesion

Assoc’d stupor or coma
– w/o might be C1-C5 lesion!

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8
Q

Opisthotonus

A

dorsiflexion of head/neck

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9
Q

De-Cerebellate Rigidity

A

Opisthotonus + rigid thoracic limbs + hip flexion

indicates Acute Cerebellar lesion

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10
Q

Schiff-Sherrington posture

A

Pelvic limbs flexed normally
w/ Thoracic limbs spastic, in rigid extension.

  • indicates Severe spinal injury (no prognostic significance)
    • T3-L3 UMN lesion
  • loss of ascending inhibition from bordering cells in spinal cord to thoracic limbs –> hypertonicity
  • Thoracic = neuro normal
  • Pelvic = UMN paresis/plegia + CP deficits
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11
Q

Sensory Ataxia

A

loss of proprioceptive pathway
• incoordination
• crossing over
• knuckling

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12
Q

Vestibular Ataxia

A

loss of vestibular pathway
• Head tilt
• Leaning
• wide based stance

Bilateral –> Wide swaying of head side to side

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13
Q

Cerebellar ataxia

A

Loss of cerebellar mediation
• Wide based stance
• dysmetria (hypermetria)
• intention tremor

– no scuffing/knuckling

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14
Q

Intention tremors

A

Coarse Tremor, Low frequency
• worsens w/ movement & goal-diretion
• cerebellar dysfunction

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15
Q

Physiologic Tremor

A

Fine Tremor, fast
• ↑ w/ weight-bearing
• not aggravated w/ movement

Caused by:

  • Hypothermia
  • Weakness
  • ↑ catecholamines (physiologic/pathologic)
  • Metabolic dz (hypoglycemia)
  • Peripheral neruopathy
  • drugs
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16
Q

Parkinsonian Tremor

A

Resting Tremor (constant), Medium frequency
• improves w/ movement
• head-bobbing

  • Dobermans w/ Droperidol
17
Q

myoclonus

A

Rhythmic jerking of a muscle group

  • hiccups
  • canine distemper virus infection
18
Q

Myotonia

A

delayed relaxation of muscle after voluntary contraction

• percussion of myotonic muscle –> dimple appearance

19
Q

What is the main differentiation btwn ataxia & paresis?

A

Muscle strength

20
Q

Reflex scale

A
0 = absent
1 = hyporeflexive
2 = normal
3 = hyperreflexive
4 = hyperreflexiv w/ clonus 
        • repeated flex/extension of join in response to a single stimuli
21
Q

Seizure

A

Paroxysmal brain dysfunction
- excessive hypersynchronous neuronal discharge

• A sign, not a disease!

22
Q

Epilepsy

A

Recurrent seizures due to intracranial dz
1 - Primary
2 - Familial
3 - Secondary = structural lesion
4 - Cryptogenic = probable lesion, but can’t see it yet
5 - Reactive epilepsy = metabolic, toxin, inflamm

23
Q

Components of seizure

A

Prodrome
Aura
Ictus
Post-ictal period

24
Q

Prodrome

A

characteristic behavior prior to onset

25
Q

Aura

A
  • Stereotypic behavior
  • autonomic activity
  • unusual psychic events
26
Q

Ictus

A
  • Involuntary muscle tone
  • Autonomic signs
  • Abnormal sensation
27
Q

Post-ictal

A
  • disoriented
  • ataxia
  • weakness
  • inappropriate U/D
  • excessive hunger/ thirst
  • agression
  • blindness
  • sensory/motor abnormalities
28
Q

Generalized seizures

A

1 - Grand mal (Clonic-tonic)

2- Petit mal (Absence) - mild

29
Q

Partial seizures

A

Simple partial
• conscious w/ focal motor activity

Complex
• unconscious w/ focal motor activity
• Psychomotor
     - abnormal sensory / behavioral activity
     - limbic/occipital
30
Q

Cluster seizures

A

2+ in 24hrs

31
Q

Status epilepticus

A

Lasting > 5 mins
OR
3+ seizures w/o return to normal consciousness between

32
Q

Seizure pathophysiolgy

A

1 - Neurotransmitter disorder
• GABA = inhibitory NT
• Glutamate = excitatory NT

2 - Ion channelopathy
• Excessive Na
• Blocked K
• Altered Ca flow