tremor and movement Flashcards

1
Q

rest tremor ddx

A

parkinsons disease

otehr akinetic rigid syndromes

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2
Q

postural (action ) tremor ddx

A

(maximal with maintained posture)

Essential tremor
physiological: anxiety, hyperthyroid, beta agonists

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3
Q

kinetic (intention) tremor ddx

A

(maximal during movement)

cerebellar diseases: MS, hereditary ataxias, tumours, strokes

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4
Q

features of essential tremor:

A

progressive
mainly symmetrical
usually absent at rest and present during posture and intentional movements (worsens with movement eg writing)
can also involve head, ajw, voice

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5
Q

is essential tremor absent at rest?

A

yes

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6
Q

what is dystonia

A

movement disorder characterised by sustained involuntary contractions of agonist and antagonist muscles, often leading to repetitive twisting movements and abnormal postures of the trunk, extremities etc

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7
Q

aetiology of dystonias

A

genetic (primary)
Spinocerebellar degenerations, HUntingtons
WIlson’s disease

Secondary
lesions in basal ganglia
drugs: antipsychotics, dopamine antagonists
post-truama

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8
Q

neurological findings in cerebellar disorders`

A

General: Intention tremor

Neurological:  
Ataxic gait, 
truncal ataxia, 
hypotonia, 
pendular reflexes, 
dysmetria, 
dysdiadochokinesis, 
nystagmus, 
dysarthria, 
heel-shin ataxia
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9
Q

causes of unilateral cerebellar syndrome

A
  1. SOL
  2. vertebrobasilar ischaemia
  3. MS
  4. Trauma
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10
Q

causes of bilateral cerbellar syndrome

A
  1. Alcoholic cerebellar degeneration
  2. Posterior fossa space-occupying lesion
  3. Multiple sclerosis
  4. Brainstem vascular lesion
  5. Inherited ataxias (Friedreich’s)
  6. Paraneoplastic syndromes
  7. Drugs (phenytoin)
  8. Hypothyroidism
  9. Arnold-Chiari malformation (NPHC)
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11
Q

unilateral cerebellar lesions will affect what part of the body?

A

ipsilateral limbs with relative truncal sparing

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12
Q

vermian cerebellar lesions will affect what part of the body

A

truncal, with relatively spared limbs

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13
Q

additional findings in alcoholic cerebellar degeneration

A

stigmata of liver disease

peripheral neuropathy

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14
Q

additional findings in Friedereich’s ataxia

A

pes cavus
pyramidal and dorsal column signs in the legs
DEPRESSED ANKLE JERKS WITH EXTENSOR PLANTARS

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15
Q

what primary tumours can affect cerebellum

A

astrocytomas

medulloblastomas

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16
Q

friedreichs ataxia aetiology

A

Autosomal recessive

chr9 &raquo_space; trinucleotide expansion&raquo_space; protein frataxin deficiency

17
Q

friedreichs ataxia Sx

A

BILATERAL cerebellar syndrome
sensorineural deafness (?hearing aids)
Diabetes (?finger pricks, fundi fro retinopathy)
optica atrophy (fundi&raquo_space; pale optic disc)
Hypertrophic cardiomyopathy (jerky pulse, double apex beat, systolic murmur)
High arched palate

losss of dorsal columns (ROMBERGS POSITIVE)
Pyramidal weakness

Mentation normal

18
Q

ddx for absent knee & ankle jerks BUT EXTENSOR PLANTARS

A
Combination:
a) peripherl neuropathy 6 stroke
b) peripheral neuropathy + cervical spondylosis
c) cervical and lumbar spondylosis
Subacute combined spinal cord degeneration
tebes dorsalis
conus medullaris lesion
friedreichs ataxia
MND
19
Q

DDx for high arched palate

A

Marfans
Turners
Friedreichs
tuberous sclerosis

20
Q

DDx for spastic and ataxic paraparesis (UMN + cerebellar signs)

A
Spinocerebellar degeneration
Arnol Chiari malforamtion
MS
syringomyelia
infarction in upper pons or internal capsule)