DEGENERATIVE BRAIN DISEASE Flashcards

1
Q

MULTIPLE SCLEORSIS

A

Demyelination of axons that connects parts of brain that progresses to functional loss

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2
Q

What genetics are more susceptible

A

twins

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3
Q

MS symptoms

A

muscle weakness
visual disturbance
paraesthesia
autonomic dysfunction
dysarthria (difficulty speaking)
pain
balance/ hearing loss

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4
Q

MS signs to a clinician

A

muscle weakness
spasticity
altered reflexes
tremor
optic atrophy
proprioceptive loss
loss of touch

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5
Q

MS investigations

A

magnetic resonance imaging
CSF (cerebro fluid) analysis
visual evoked potentials

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6
Q

what is the result of a CSF analysis in someone with MS

A

reduced lymphocytes
increased IgG protein

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7
Q

is there a cure for MS

A

NO

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8
Q

how do you systemically manage MS

A

antibiotics
antispasmodics
analgesia; physiotherapy and occupational therapy

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9
Q

the 2 types of MS

A

relapsing and remitting
primary progressive

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10
Q

describe the relapsing and remitting type of MS

A

acute exacerbations and periods of respite
damage builds up with each episode and then develops to progressive form

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11
Q

describe the primary progressive type of MS

A

slow and steady progressive deterioration
cumulative neurological damage

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12
Q

what drugs can slow down the progressive form on MS

A

disease modifying therapies:
- cladribine
- siponomod
- ocrelizumab

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13
Q

what treatment can ‘reboot’ the immune system

A

stem cell transplant

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14
Q

dental aspects of MS

A

limited mobility
orofacial motor and sensory disturbance
chronic orofacial pain
enhanced risk of trigeminal neuralgia

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15
Q

degeneration of anterior horns of the corticospinal tracts in the spinal cord

A

motor neurone disease

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16
Q

common age to have motor neurone disease

A

30-60

17
Q

motor neurone disease mortality

A

3 years after diagnosis

18
Q

symptoms of motor neurone disease

A

progressive loss of motor function in the:
- limbs
- intercostal
- diagphragm
- motori CNVII - XII

19
Q

signs of motor neurone disease

A

weakness in ankle/ leg
slurred speech
difficulty swallowing food
weak grip
muscle cramps and twitches
weight loss in arms and leg muscles
emotional liability

20
Q

treatment for motor neurone disease

A

physiotherapy and occupational therapy
riluzole: 6-9 months life extension
aspiration prevention with PEG tube feed

21
Q

dental aspects of motor neurone disease

A

difficulty to accept dental care
muscle weakness of head and neck
medication that reduces saliva (anticholinergics)
may have Botox in salivary glands
drooling and swallowing difficulties

22
Q

Degeneration of dopaminergic neurons in the basal ganglia of the brain (lack of dopamine)

A

parkinsons disease

23
Q

what does parkinsons result in

A

difficulty of message passing from thinking to doing

24
Q

clinical features of parkinsons

A

bradykinesia; slow movement and slow initiation of movement
rigidity; increased muscle tone
tremor; slow amplitude - common in mandible

25
Q

key feature of parkinsons

A

rest tremor

26
Q

parkinsons manifestations

A

impaired gait (unsteady walking) and falls
mask-like face (flat looking)
swallowing problems

27
Q

medical treatment of parkinsons

A

dopaminergic drugs; direct replacement of dopamine or agonists

28
Q

medical form of dopamine

A

levodopa

29
Q

dopamine analogues (tablets)

A

promipexole
selegilline

30
Q

dopamine analogues (subcutaneous injection)

A

apomorphine

31
Q

dopamine analogues (infused directly into gut)

A

duodopa

32
Q

surgical tx for parkinsons

A

stereotactic surgery - deep brain stimulation; electrode into the brain

stem cell transplant

33
Q

dental aspects of parkinsons

A

difficulty accepting tx
tremor at rest; reduces mouth opening
dry mouth; from anticholinergics
potential drug interactions