MS/MND/spinal cord/muscular disorders Flashcards

1
Q

Proportion of patients with relapsing-remitting MS who go on to develop secondary progressive?

A

65%

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2
Q

Management of MS? (2)

A

Disease-modifying drugs e.g. Interferon beta, fingolimod

MePred 0.5g daily for flares

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3
Q

What does MND never involve? (2)

A

Eye movements

Sensory nerves

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4
Q

Prognosis of MND?

A

Death from ventilatory failure usually within 3-5 years after diagnosis

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5
Q

Only disease-modifying drug licensed for MND?

A

Riluzole- confers a survival benefit/delays time to mechanical ventilation

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6
Q

Symptom control in MND: cramps

A

Quinine (1st line)

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7
Q

Symptom control in MND: spasticity

A

Baclofen, tizanidine, dantrolene, gabapentin

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8
Q

Symptom control in MND: drooling

A

Propantheline, glycopyrronium bromide, amitriptyline, botox

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9
Q

Symptom control in MND; dysphagia

A

Discuss parenteral feeding e.g. PEG

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10
Q

Three forms of CJD?

A

Sporadic (“classical”)
Variant- (from ingestion of nervous tissue in beef with bovine spongiform encephalitis)
Familail prion disease

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11
Q

Injury to the spinal cord above T1 causes?

A

Quadriplegia/tetraplegia

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12
Q

Injury to the spinal cord below T1 causes?

A

Paraplegia

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13
Q

Ipsilateral movement loss with contralateral pain and sensation loss?

A

Brown-Sequard syndrome

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14
Q

Wasting + weakness of hands and arms, with loss of temperature + pain sensation in a “cape” distribution

A

Syringomyelia

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15
Q

Inflammation of the spinal cord at a single level

A

Transverse myelitis

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16
Q

Cafe-au-lait patches?

A

Type 1 neurofibromatosis

17
Q

Bilateral acoustic neuromas?

A

Type 2 neurofibromatosis

18
Q

Inheritance of NF?

A

Autosomal dominant

19
Q

First-line investigation in restless legs syndrome?

A

Serum ferritin

20
Q

Management of restless legs?

A

Dopamine agonists e.g. pramipexole, ropinorole

21
Q

Nystagmus + opthalmoplegia + ataxia

A

Wernicke’s encephalopathy