Neyrological System Flashcards

1
Q

Dysarthria

A

Impaired speech due to weakness of the muscles that control speech

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2
Q

Dysphasia or aphasia

A

Impaired or absence of the ability to speak due to neurological abnormalities

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3
Q

Dysgraphia or agraphia

A

Impaired or absence of the ability to write

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4
Q

Dyspraxia or apraxia

A

impaired or absent ability
to perform purposeful movements in the
absence of paralysis.

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5
Q

Glasgow coma scale

A

Eyes
Open spontaneously 4
Open to command 3
Open to pain 2
Do not open 1
Speech
Sensible/orientated 5– what’s your name, where are you, what month is it?
Confused 4– speaking in phases or relatively complete sentences
Inappropriate words 3–
Incomprehensible sounds 2
None 1
Motor
Obeys commands 6
responses Localizes stimuli 5
Withdraws from stimuli 4
Flexion responses or deCORticate 3
Extension responses or dEcErEbratE meaning the brain stem is affected 2
None 1

EVM-456

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6
Q

Things that can affect GCS

A
  • paralyzed patient can’t check for motor
  • intubation : verbal affected
  • injuries to the bone
  • swelling
  • sedation
  • hearing problems
  • mental deficits
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7
Q

Deep vein thrombosis

A

Risk factor for DVT:
- recent surgery
- immobility
- long travel
- pregnancy
- hormone therapy with estrogen eg COC
- cancer
- thrombophilia
- systemic lupus eeytgematous
- polycythemia

Causes : numerous but remember antiphospholipid syndrome

Presentation: calf or leg swelling, dilated superficial veins, tenderness, colour change to the leg, oedema

Hx: risk factors + risk of PE (shortness of breath, palpitations, pleuritic chest pain)

Diagnosis: D-diner (but it’s not specific)

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8
Q

Ataxic gait Ddx

A

Cerebellar disease
Acute alcohol intoxication
Migraine
Post traumatic/post concussive
Multiple sclerosis

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9
Q

Hemiplegic gait Ddx

A

Vascular diseases: stroke, diabetic neuropathy
Infective: encephalitis, meningitis, brain abscess
Traumatic brain jnjury
Congenital: cerebral palsy
Multiple sclerosis

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10
Q

Disease process affecting both the myelin and neurons (neurodegenration)

A
  • stroke
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11
Q

Disease process affecting only the myelin sheath

A
  • multiple sclerosis
  • Guillean Barre syndrome
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12
Q

Lower motor neuron lesion presentation

A
  • lower motor neuron lesion (i.e., injury of anterior
    horn cells and/or the peripheral nerve(s) in which
    their axons travel)
  • The muscle(s) would be paralyzed and would be floppy (flaccid).
  • Reflexes would be diminished or lost.
  • The muscle would no longer be under any control, and left
    to its own devices it would twitch (fasciculate).
    -The classic symptoms of a lower motor neuron lesion are flaccid paralysis, diminished or absent reflexes, fasciculations, and, over time, muscle atrophy.
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13
Q

Upper motor neuron lesion presentation

A
  • The affected muscles become paralyzed.
  • In addition, because of the
    loss of higher control, the lower motor neuron fires spontaneously, causing spasm in the affected muscles,
    a state of tonic contraction.
  • With this loss of inhibition
    from above, reflexes eventually become exaggerated or
    hyperactive.
  • Also, primitive reflexes can resurface because of the loss of upper motor neuron inhibition.
  • One example is Babinski’s sign. If you stroke the bottom of the foot, the toes should normally curl down. If the big
    toe goes up, this is Babinski’s sign, and is abnormal in
    adults.
    NB: Babinski’s sign indicates an upper motor neuron lesion anywhere from the motor cortex through the corticospinal tract’s path in the brainstem and spinal cord.
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14
Q

Lower motor neuron lesion presentation summary

A
  • weakness or paralysis
  • Flaccidity and decreased reflexes
  • fasciculations
  • muscle atrophy (severe)
  • decreased tone
  • distribution of weakness distal or segmental
  • Babinski sign absent
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15
Q

Corticobulbar tract supplies

A

The brain stem
Synapses at the upper part of the medulla

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16
Q

Upper motor Neuro is made up of

A
  • corticospinal tract
  • corticobulbar tract
17
Q

Components of LMN

A
  • somatic motor neuron
  • bulbar motor neuron
18
Q

Upper motor neuron presentation summary

A
  • weakness or paralysis
  • spasticity
  • Increased reflexes
  • positive Babinski sign
  • atrophy (none)
  • fasciculations (none)
    Distribution of weakness (pyramidal- in the upper limb extensors are more weak and in the lower limb flexors are more weak/regional)
19
Q

UMN Neurodiseases

A

Sporadic: primary lateral sclerosis
Heeditary: hereditary spastic paraplegia
Amyotrophic lateral sclerosis

20
Q

LMN diseases

A

Sporadic : progressive muscular atrophy, polio, West Nile virus
Hereditary: spinal muscular atrophy, spinobulbar muscular atrophy (Kennedy disease)
Amyotrophic lateral sclerosis

21
Q

Headache Ddx

A
  • migraine (acute recurrent)
  • raised ICP such as tumour, abscess, hydrocephalus, ICP hypertension(subacute progressive)
  • infections: meningitis, encephalitis (subacute progressive)
  • medication overuse such as analgesia (chronic)
  • drugs such as nitrates, dipyridamole
  • subarachnoid haemorrhage (acute single episode)
  • idiopathic intracranial hypotension (acute single episode)
  • cerebral vein thrombosis (acute single episode)