Moevment Disorders Flashcards

1
Q

Asterixis

A

Uncontrolled Extension of the wrists which results in a “flapping of the wrists”

Seen in:

  • hepatic encephalopathy
  • Wilson disease
  • metabolic disorders
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Athetosis

A

Slow undulating snake-like movements usually in the fingers and hands

Seen in:

  • lesions of the basal ganglia
  • degenerative disorders
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Blepharospasm

A

A type of dystonia that affects only the eyes
- uncontrolled blinking or eyelid movement

Seen in:

  • some medications
  • OD of medications
  • genetic defects
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Chorea

A

Uncontrolled sudden jerking or dance-like movements

Seen in:

  • lesions to the basal ganglia
  • Huntington’s
  • rheumatic fever
  • Wilson’s disease
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Dystonia

A

Sustained muscle contractions that are uncontrolled

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Hemiballsmus

A

Uncontrolled flailing/flinging motions of the extremities

Seen in:

  • lesions to the contralateral STN
  • lacunar strokes
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Tardive dyskinesia

A

Controlled repetitive Orofacial movements (usually smacking of lips or abnormal tongue movements)

Seen in:

  • dopamine antagonist uses
  • absence seizures
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Torticolis

A

Sustained muscle contractions of the neck similar to dystonia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Huntington’s disease

A

A type of hyperkinetic movement disorder

Is a autosomal dominant w/ complete penetrance disease that results in a CAG triplet on chromosome 4 and repeat expansions of HTT genes on chromosome 4

Results in corpus striatum atrophy which lowers number of GABA neurons in the corpus striatum and reduced inhibitory output from the striatum

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Clinical features of Huntington’s

A

Doesn’t show until 30-50s usually

Clinical features:

  • chorea
  • dysarthria
  • dysphagia
  • abnormal eye movements
  • neurobehavioral disorders
  • dementia

*(Is autosomal dominant)

Diagnosis:

  • family history/ genetic testing
  • symptoms
  • CT/MRI

Treatment:

  • D2 antagonists
  • mood medications
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Restless leg syndrome

A

Hyperkinetic disorder

Etiology

  • genetics
  • iron deficiencies
  • diabetic neuropathy
  • uremia
  • OSA
  • pregnancy

Symptoms

  • leg sensations (akathisa) that worsen at night
  • symptoms are present only at rest, movement makes it better

Diagnosis

  • polysomnography
  • history
  • labs

Treatment
- treat underlying cause

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Types of tremors

A

Postural:
- occurs when the body part is voluntarily maintained against gravity

Action:
- occurs with voluntary contraction of muscles

Kinetic:
- occurs with any form of voluntary movement

Intention:

  • subtype of kinetic tremor amplified as the target is reached
  • always implies direct or pathway lesions of the cerebellum

Rest:

  • occurs in a body part that is relaxed and completely supported against gravity
  • usually implies Parkinsonism
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Essential tremor (familial)

A

Hyperkinetic disorder

Most common type of tremor

50% of the time is autosomal dominant genetic caused

High frequency quick tremors that usually affects only the upper extremities (Can affect face and voice however)

Clinical features:

  • bimodal distribution that results in bilateral, postural or kinetic tremors.
  • usually one hand is worse (although this isnt usually clinically relevant)
  • alcohol actually fixes these tremors

Treatments:

  • life style modifications
  • BBs
  • anti-epileptics
  • thalamic surgery (severe cases only)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Wilson’s disease

A

hyperkinetic disorder

Autosomal recessive disorder of copper metabolism
- excessive build up of copper since it cannot bind to ceruloplasmin (its transfer protein)

Clinical features

  • people under 40 yrs
  • hepatic issues
  • action tremors
  • asterixis
  • *presence of kayser-flesicher rings (brown ring on the outside edge of the iris)
  • hemolytic anemia
  • behavioral disturbances

Diagnosis

  • elevated urinary copper
  • low ceruloplasmin
  • genetic testing

Treatment:
- penicillamine (chelating agent that binds to coppe)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Parkinson’s disease

A

Hypokinetic disorder that is the 2nd most common movement disorder

Degeneration of the substantia Nigra and respective dopamine neurons
- results in inability to inhibit GABA output from the striatum (net negative for movement)

Causes

  • genetic neurodegenerative
  • therapeutic drugs in high doses
  • toxins
  • post traumatic stress and trauma

Symptoms:

  • unilateral/slow frequency resting tremors
  • cogwheel rigidity*
  • akinesia/ bradykinesia
  • mask-like faces
  • hypotonia
  • dysphagia
  • micrograph is
  • postural instability w/ shuffling gate
  • autonomic dysfunction
  • cognative and behavioral dysfunctions
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is a DaT scan?

A

Shows areas of the brain that are “hotspots” for dopamine uptake

Used to diagnose Parkinson’s
- will show decreased DaT activity over time and in areas where it should be high