Neurology-Movement-Disorders-and-others Flashcards

1
Q

Types of tremors: 5

A
  1. Resting
  2. Postural
  3. Action
  4. Postural-action
  5. Intention

Rhythmic and oscillatory movement of a body part with a relatively constant frequency and variable amplitude. It is caused by either alternating or synchronous contractions of antagonistic muscles

Tremors may be broadly classified into resting, postural, action, postural-action, and intention tremors

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2
Q

Tremor present when holding up a newspaper versus when pouring a cup of tea

A

Postural versus Action

Postural tremors occur with the body part suspended against gravity. Action tremors remain unchanged during the course of a voluntary movement.

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3
Q

also known as cerebellar tremor, is a dyskinetic disorder characterized by a broad, coarse, and low frequency (below 5 Hz) tremor. The amplitude increases as an extremity approaches the endpoint of deliberate and visually guided movement

A

Intention tremor

(kinetic tremor subtype)

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4
Q

involuntary, rhythmic oscillations of one or more body parts

A

Tremor

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5
Q

Differentiate ET from Parkinsons’: parameters

A
  1. Laterality: Parkinson’s is unilateral
  2. Action vs rest
  3. Alcohol response: improves ET, no effect in Parkinson’s
  4. Speed: Fast (6-10) hz, Slow (4-6) hz
  5. Movement: flexion-extension, pill rolling
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6
Q

Which tremor has a genetic component?

A

ET

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7
Q
  1. Involuntary excessive muscle contractions that tend to be sustained and patterned,
  2. initiated or worsened by voluntary action and associated with overflow muscle activation
  3. abnormal postures or movement
  4. dysfunction of the basal ganglia, cerebellum, cortex
A

Dystonia

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8
Q

Drug groups causing dystonias

A
  1. Anti-emetics
  2. Anti-psychotics
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9
Q

Stroke in this part can cause dystonia

A

Putamen

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10
Q

Dystonia classification basis

A

Body part affected

Eg: spasmodic dysphonia: vocal cords,

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11
Q

Treatable causes of dystonia

A
  1. Wilson’s
  2. Dopa-responsive dystonia
  3. DYT1 gene–associated dystonia
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12
Q

Rx: focal dystonias

A

Botulinum

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13
A

This is a transverse section of the striatum from a structural MR image. The striatum includes the caudate nucleus (top) and putamen (right) and the globus pallidus (left).

The putamen and caudate nucleus together form the dorsal striatum.

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14
Q

Involuntary, irregular, unpatterned, and unsustained movements with variable timing and distribution

A

Chorea

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15
Q

Involuntary slow and irregular writhing movements most often affecting the distal limbs

A

Athetosis

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16
Q

Involuntary, large-amplitude, flinging movements, typically involving proximal muscles that move an entire limb

A

Ballism

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17
Q

Autosomal dominant inheritance with gene test for triplet nucleotide repeat. Chorea, psychiatric symptoms, and cognitive dysfunction progress over 10 to 20 years until death.

A

Huntington

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18
Q

Strokes in this basal ganglia nucleus will cause choreoathetoid movements

A

sub-thalamic

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19
Q

disorder of childhood resulting from infection via Group A beta-hemolytic streptococcus (GABHS), characterized by rapid, irregular, and aimless involuntary movements of the arms and legs, trunk, and facial muscles

A

Sydenham’s chorea

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20
Q

Prognosis of chorea from stroke

A

Ofent improves on its own

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21
Q

Drug-induced movement disorders can include

A
  1. Tremor
  2. Parkinsonism
  3. Choreoathetosis
  4. Acute dystonia
  5. Tardive dystonia
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22
Q

Tetrabenazine

A

symptomatic treatment of hyperkinetic movement disorders

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23
Q

Involuntary, abrupt, brief and jerky movement of a body part. Often described as “lightning fast.”

A

Myoclonus

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24
Q

What sort of involuntary movement is a hiccup?

A

Myoclonus

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25
Jerky movements when falling asleep
Hypnic jerks
26
Lance-Adams syndrome
Post-hypoxic myoclonus
27
Asterixis is a type of:
Myoclonus
28
Unverricht-Lundborg disease,neuronal ceroid lipofuscinoses, sialidosis, and Lafora body disease are all:
Myoclonic epilepsies The one that was left out: myoclonic epilepsy with ragged red fibers,
29
Brief stereotyped movements, preceded by an urge, followed by a sense of relief,
Tic
30
Tourette syndrome: Multiple motor and vocal tics beginning before age _ and lasting for at least _ months
Tourette syndrome: Multiple motor and vocal tics beginning before age 18 and lasting for at least 6 months
31
Which movement disorder is associated with: Iron deficiency anemia, end-stage renal disease, pregnancy, peripheral neuropathy, lumbar radiculopathy, autoimmune disorders, vitamin B12, folate, or magnesium deficiencies
Secondary Restless Legs Syndrome
32
sympatholytic drug used in the treatment of attention deficit hyperactivity disorder (ADHD), anxiety and hypertension
Guanfacine
33
Parkinsonism
1. **bradykinesia** 2. rest tremor 3. rigidity 4. postural instability Most sensitive: Bradykinesia is a generalized slowness of movement, and is present at onset of PD in approximately 80 percent of patients [17]. It is arguably the major cause of disability in PD and is eventually seen in almost all patients.
34
Difference between Parkinsonism and Parkinson's
Parkinsonism :collection of symptoms that can have many different etiologies Parkinson disease: specific disorder that is the most common cause of parkinsonism
35
Parkinsonism, gaze palsies, slow saccades, imbalance with falls, dysarthria, or truncal dystonia
PSP
36
Parkinsonism, early dementia, fluctuating alertness, early visual hallucinations
Dementia with Lewy bodies
37
Parkinsonism, asymmetrical stiffness, apraxia, or dysfunction of one arm, dysarthria, or dementia
Corticobasilar degeneration
38
Parkinsonism, early autonomic dysfunction, sometimes cerebellar ataxia
MSA
39
Prominant gait dysfunction (imbalanced, slow, feet sliding on ground), dementia, urinary incontinence, possible parkinsonism
NPH
40
Parkinsonism of the lower body more than upper body, prominent gait disability, cognitive dysfunction (or dementia)
Vascular parkinsonism
41
Accumulation of small or large strokes that may produce parkinsonism more centered in the lower half of the body
Vascular parkinsonism
42
Parkinson's disease is caused by the progressive degeneration of dopaminergic neurons within the:
substantia nigra
43
[Where is the substantia nigra?](http://en.wikipedia.org/wiki/Substantia_nigra#/media/File:Substantia_nigra.gif)
Midbrain
44
Aetiologyof Parkinson's
Most are idiopathic
45
Parkinson's disease: Rx
1. Carbidopa/levodopa (Sinemet) is still the most effective treatment. Typically: complicated by wearing off and dyskinesias. 2. Dopamine agonists: Pramipexole, ropinirole. These have longer lasting effects than carbidopa/levodopa but usually more side effects, especially in the elderly. 3. MAO-B inhibitors: Selegiline, rasagiline. Mild benefits but may prolong the per dose benefits of carbidopa/levodopa. Some neuroprotective effects. 4. Catechol-O-methyltransferase (COMT) inhibitors: Entacapone + carbidopa/levodopa prolongs the effect. Tolcapone also may be used though hepatic monitoring is required. 5. Amantadine: Weak
46
Deep brain stimulation Rx of Parkinson's disease: stimulation of the
subthalamic nucleus or the globus pallidus
47
A motor and behavioral dysregulation syndrome with the inability to move despite full physical capability, with difficulty initiating and terminating movement. Postures become frozen or oddly positioned, and actions become contrary to intent.
Catatonia
48
Examples of catatonia occur non-psych conditions
1. Drug intoxication 2. Tumor 3. Encephalitis 4. Post-liver transplant
49
Forms of catatonia
Hypokinetic, Excited, Malignant
50
Effect of benzodiazepines on catatonia
Improves symptoms within minutes
51
Dysfunction in performing learned, skilled movements that is not due to primary neurologic dysfuntions such as weakness, sensory loss, changes in posture or tone, incoordination, or impaired attention, comprehension of the task, or cooperation
Apraxia
52
Apraxia localization
parietal lobes, frontal lobes, and their subcortical connections
53
Incoordination arising from dysfunction in timing, rhythm, accuracy (targeting), and smoothness of movement
Ataxia
54
Ataxias are usually due to abnormalities in the __ or its motor and/or sensory pathways (\_\_ ataxia)
usually due to abnormalities in the cerebellum or its motor and/or sensory pathways (spinocerebellar ataxia)
55
Irregular timing or trajectory of targeted movements
Dysmetria
56
Breakdown of the normal timing and sequencing of rapid alternating movements
Dysdiadochokinesis
57
Common symptoms include imbalance, wide-based gait, falls, dysarthria, eye movement abnormalities, intention tremor, and mistargeting with the limbs (trouble pouring water, poor handwriting, knocking over objects, etc.)
Ataxia ie: 1. Stroke to cerebellum or brainstem 2. Autoimmune: Includes celiac disease, anti-GAD syndrome, Miller Fisher syndrome 3. Inherited disorders: Spinocerebellar ataxia, Friedreich ataxia, ataxia-telangiectasia, 4. Metabolic/toxic: Vitamin E deficiency, hypothyroidism, chronic alcoholism 5. Antiepileptics 6. Infections 7. Tumor/mass, or paraneoplastic/parainfectious
58
A 38-year-old man with an unknown psychiatric history is brought to the emergency room for bizarre behavior. While waiting for the psychiatry resident to evaluate the patient, you are asked by the nurses to give him haloperidol to control his behavior, as he is placing the staff at risk. Twenty minutes later you are called to see him because the patient became stiff and unable to speak, with his eyes rolling back in his head and his jaw and neck stiffening. He has remained conscious throughout this episode. Appropriate treatment at this time would be Phenytoin Lorazepam Risperidone Diphenhydramine
Diphenhydramine Dx: acute dystonic reaction from haloperidol. Patients with acute dystonic reaction maintain consciousness.
59
Central vertigo: SySx
1. Persistent: No change with position 2. Directional nystagmus 3. Severe truncal instability 4. Negative head thrust
60
Vestibular neuritis vs BPPV
1. BPPV: symptoms caused by head motion. 2. BPPV: Recurrent 3. BPPV: symptoms last seconds 4. VN: Single, acute episode, 5. VN: head thrust +ve 6. VN: prodromal viral infection
61
Vertigo: causes
1. BPPV 2. VN 3. Meniere's 4. Vestibular migraine 5. Brainstem CVA 6. Vertebrobasilar TIA 7. Cerebellar CVA
62
Vertigo: Peripheral causes
1. BPPV 2. VN 3. Meniere's
63
Vertigo: Central causes
1. Vestibular migraine 2. Cerebellar TIA/CVA 3. Brainstem CVA
64
Vasomotor rhinitis with prominent watery rhinorrhea: Rx
Ipratopium nasal spray
65
Vasomotor rhinitis
Nonallergic rhinitis (NAR) is a syndrome in which some combination of sneezing, rhinorrhea, nasal congestion, and postnasal drainage is present over time without a specific cause. The pathogenesis is not known. Other terms for this condition include vasomotor rhinitis, idiopathic rhinitis, nonallergic-noninfectious rhinitis, and intrinsic rhinitis.
66
Vasomotor Rhinitis: Rx
1. mild symptoms: intranasal glucocorticoid (INGC) or an intranasal antihistamine spray 2. Moderate-to-severe symptoms: INGCs + intranasal antihistamine 3. ipratropium nasal spray for patients with prominent watery rhinorrhea without other symptoms 4. NAR and prominent nasal congestion: azelastine, Pseudoephedrine PRN Neti pot
67
keratinized, desquamated epithelial collection in the middle ear or mastoid and may occur secondary to tympanic membrane perforation, but also may occur as a primary lesion.
Cholesteatoma
68
Vertigo: recurrent episodes lasting less than a minute
BPPV
69
Vestibular migraine vs BPPV
1. Vestibular migraine symptoms last longer. 2. VM: dx requires accompanied by aura or migraine headache