Neuro Flashcards

1
Q

Motor pathway description?

A

Primary motor cortex -> UMN moves to medulla here 90% lateral corticospinal tract decussate and 10% dont anterior corticospinal tract -> Move down until they reach the correct spinal level at which they synapse with the LMN which innervates the relevant muscles

Corticospinal tracts aka pyramidal tract

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2
Q

What is UMN leisons, what about LMN - motor?

A

UMN:
Brain
Brainstem
Injury to white matter of spinal cord up to level of synapse

LMN:
Injury to grey matter at the level of the synapse (anterior horn) + injury to axons leaving the spinal cord

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3
Q

Why do you get the sx you do in UMN leisons?

A

There is no UMN control of the LMN hence this response is NOT controlled

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4
Q

What are UMN and LMN sx?

A
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5
Q

What are some possible differentials for Hemiplegia?

A

Vascular:
- Stroke
- TIA (signs would last less than 24h and no evidence of infarction upon brain imaging)

SOL

Demyelinating conditions eg MS
- Signs and sx disseminated in time + space (can be motor, sensory and cerebellar)

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6
Q

What ix would you like to do further support stroke dx?

A
  • CN exam - may notice eyebrow sparing facial nerve palsy
  • Assess CV RFs - checking for signs of AF, carotid bruits and check for any heart murmurs
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7
Q

How can strokes be classified?

A

Due to pathophysiology:
- Ischaemic
- Haemorrhagic (15%)

Bamford classification - location:
- Total anterior circulation stroke - highest mortality
- Partial anterior circulation stroke
- Posterior circulation stroke
- Lacunar stroke

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8
Q

Describe the sensory pathway:

A

Involves Dorsal column (touch, vibration and proprioception) and Anterolateral spinothalamic (pain and temprature) tract

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9
Q

What are the possible causes of Peripheral Neuropathy?

A

Predominatlty sensory:
ABCDE
Alcohol and diabetes = most common
Vit B12 deficiency
Chronic renal failure + Ca (paraneoplastic)
Drugs eg isonisaid or vincristine
Every vasculitidies (eg SLE) + Everything else (eg paraneoplastic)

Predominantly motor:
- Charcot Marie Tooth - both sensory and motor however more likely motor -> young, high arched foot and champage bottle lower limbs mutation in PNP22 gene
- GBS - if acute
- Chronic inflammatory demyelinateing polyneuropathy - if more chronic

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10
Q

How can you ix peripheral neuropahty?

A

Bedside:
- Blood glucose
- Urine dip - check for glucose

Bloods:
- DM - fasting glucose, HbA1c
- Alcoholc - FBC, LFTs, clotting
- Chronic renal failure - U+E
- Vitamin deficiency - B12 and Folate
- Vasculitidies - ESR and autoantibody screens

Imaging:
- Consider XR and CT imaging to check for paraneoplastic features

Special tests:
- Nerve conduction studies
- Gene - PMP22 in CMT

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11
Q

What are some possible dx for MS and why?

A
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12
Q

What are the possible signs of MS?

A
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13
Q

Describe what is INO?

A

Leison is in the eye that cannot adduct (go in) due to pathology in medial longitudinal fasiculus

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14
Q

What are the different types of MS?

A
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15
Q

Mx of MS?

A
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16
Q

What are the 3 classical signs of parkinsonianism?

A
  • Bradykinesia
  • Pill rolling tremor
  • Rigidity
17
Q

What are the other types of Parkinsonianism?

A
18
Q

Mx of Parkinsons?

A
19
Q

What is an indication of maintenance therapy in MS (DMARD use)?

A

2 relapses in last 2 years

20
Q

What are some possible causes of proximal myopathy?

A
21
Q

What to do next when you have a pt and you suspect proximal myopathy?

A
22
Q

What are the further ix to do in proximal myopathy pt?

A
23
Q

What are the causes of Cushings?

A
24
Q

What are the signs and sx of cushings syndrome?

A
25
Q

What are some possible causes of Ptosis?

A

Elevation of eyelid involves - levator palpebrae superioris (3rd nerve) + superior tarsal muscle (sympathetic control)

26
Q

What should you do next in a pt w/ unilateral ptosis?

A
27
Q

What further ix should be in myasthenia gravis

A
28
Q

Present findings for cerebellar disease?

A
  1. On gait assessment:
    a. Broad-based gait
    b. Inability to perform heel-to-toe walking
    c. Romberg’s test
    i. If negative (i.e. not worse with eye closure) = pure cerebellar
    ii. If positive = ataxia is also due to loss of proprioceptive
    input
  2. Impaired coordination
    a. Impaired past pointing and dysdiadochokinesis
    b. Impaired heel-skin test

Relevant negative = standard + normal tone, reflexes, power, sensation

29
Q

Difference between sensory and pure cerebellar ataxia?

A

c. Romberg’s test
i. If negative (i.e. not worse with eye closure) = pure cerebellar
ii. If positive = ataxia is also due to loss of proprioceptive
input

30
Q

What extra tests are needed for myotonic dystrophy?

A

Myotonic dystrophy (pt has ↓ cognitive function = SPOT DIAGNOSIS)

  • Ask pt to shake hand and grip tightly as possible looking for delayed release when asked to let go
  • Clench teeth and feel for masseter msucle wasting
31
Q

Myotonic dystrophy presentation

A
32
Q

What extra tests are needed for myasthenia gravis + present that pt?

A
33
Q

Present findings in a CMT disease?

A