Neurosciences Flashcards

1
Q

What are typical Upper Motor Neurone Symptoms? (4)

A
  • Muscle Weakness
  • Spasticity
  • Hyperreflexia
  • Resistance to movement
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2
Q

Common tracts in the brainstem? (4)

A
  • Corticospinal tract -> motor tract
  • Spinothalamic tract -> sensory tract (pain and temperature sensation)
  • Dorsal column -> sensory tract (discriminatory touch, conscious proprioceptive information)
  • Spinocerebellar tract -> unconscious proprioceptive information
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3
Q

Which are the motor spinal tracts? (2)

A
  • Pyramidal (corticospinal e.g. voluntary movement)

- Extra Pyramidal (e.g. non-voluntary movement: balance, muscle tone, posture and reflexes)

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4
Q

What is MND?

A

Motor Neurone Disease: progressive degeneration of the motor neurones

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5
Q

What are the 3 main variants of MND?

A
  1. ALS (amyotrophic lateral sclerosis): upper and lower motor neurone signs
  2. PLS (primary lateral sclerosis): upper motor neurone signs
  3. PMA (progressive muscular atrophy): lower neurone signs
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6
Q

What is a classic onset of MND?

A

Usually loss of power of a limb e.g. clumsy hand

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7
Q

What gives you a poor prognosis?

A
  • Later age
  • Bulbar involvement
  • Short diagnostic interval
  • ALS/PMA Variant
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8
Q

Management of MND?

A
  • NIV (can improve life expectancy to up to 1yr)
  • MDT
  • Medication
  • PEG
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9
Q

What is hydrocephalus?

A

Abnormal accumulation of CSF in the ventricular system of the brain.

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10
Q

What are common symptom of hydrocephalus?

A
  • Abnormal gait
  • Urinary incontinence
  • Progressively impaired cognition
  • Nausea and vomiting
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11
Q

What is CJD?

A

Creutzfeldt-Jakob Disease

Abnormal prion proteins (part of the nervous system) collect in the brain leading to brain atrophy.

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12
Q

Main symptoms of CJD?

A
  • 1/3rd = fatigue, sleep problems, reduced appetite
  • 1/3rd = neurological problems such as behavioural changes, memory loss and confusion
  • 1/3rd = focal signs such as cerebellar ataxia, aphasia,, visual disturbance and some motor weakness
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13
Q

What is an upper motor neurone lesion?

A

Lesion of the neural pathway in the anterior horn of the spinal cord or motor nuclei of the cranial nerves.

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14
Q

What is a lower motor neurone lesion?

A

Lesion of the nerve fibres which travel from the anterior horn to associated muscles.

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15
Q

What is Myasthenia Gravis and what is its main presentation (motor/sensation/reflex)?

A

Lesion to the neuromuscular junction.
Symptoms:
- Motor fatiguability, sensation intact, normal or decreased reflexes

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16
Q

What is peripheral polyneuropathy of alcoholism and its main presentation (motor/sensation/reflex)?

A

Lesion to the peripheral nerves.
Symptoms:
- Motor weakness and atrophy more distal than proximal (sometimes with fasciculations), sensory deficits often in glove/stocking distribution, decreased relexes

17
Q

What is muscular dystrophy and its main presentation (motor/sensation/reflex)?

A

Lesions to the muscles themselves.
Symptoms:
- Motor weakness proximal>distal (fasciculations are rare), sensation intact, normal or decreased reflexes

18
Q

What is GBS and its main presentation (motor/sensory/reflex)?

A

Person’s autoimmune system attacks its own peripheral nervous system via demyelination in an ascending pattern.
Symptoms:
- Symmetrical proximal and distal motor weakness but often begins proximally in feet, sensory loss symmetrically (paraesthesia in feet > hands is often the first symptom), absent or decreased reflexes

19
Q

What is MS and its main presentation (motor/sensory/reflex)?

A

Multiple Sclerosis is the demyelination of the central nervous system (brain and spinal cord) by the person’s autoimmune system. (most commonly unilateral)
Symptoms:
- Muscle weakness, spasms (spasticity), tremors, ataxia
- Numbness, Pins and Needles, Paraesthesia
- Dysarthria, Nystagmus, Intention tremor
- Symptoms vary and depend on the location of the plaques
- Fatigue, double vision, loss of balance, loss of coordination, altered cognition

20
Q

What are the 4 main types of MS?

A
  1. Relapse-Remitting (most common)
  2. Secondary progressive (initially like relapse-remitting but over time turns into a constant deterioration)
  3. Primary progressive (constant deterioration)
  4. Progressive - relapsing (one constant attack with worsening bouts superimposed)