Hyperkinetic Dysarthria Flashcards

1
Q

Hyperkinetic Dysarthria: Overview

A

Associated with BG control circuit abnormalities

Can manifest in any/all levels of speech production; prominent in prosody and rate.

Impression that speech is being interfered with by involuntary movements that distort, slow, or interrupt its movement

Observing abnormal head, orofacial, and resp. movements facilitates diagnosis

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2
Q

Hyperkinetic Dysarthria: Characteristics

A

Deviant speech characteristics are result of abnormal, rhythmic, or irregular rapid or slow involuntary movements.

Perceptually distinguishable from other dysarthrias

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3
Q

Clinical Characteristics of BG Control Circuit Disorders Associated with Hyperkinetic Dysarthrias

A

Abnormal, involuntary movements can occur at rest, during static postures, or during voluntary movement.

Some hyperkinesias are rapid, unsustained, or unpatterned; others are slower, may be prolonged.

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4
Q

Dyskinesia

A

Term that refers to abnormal, involuntary movements regardless of etiology.

Most hereditary or acquired conditions that cause orofacial dyskinesias are associated with BG abnormalities.

Orofacial dyskinesias are a common side effect of antipsychotics.

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5
Q

Myoclonus

A

Characterized by involuntary single or repetitive brief, lightening-like jerks of a body part; jerks can be rhythmic or not.

Can be confined to a single muscle or be multifocal.

Can occur spontaneously or triggered by visual, tactile, or auditory stimuli.

Can result from TBI, encephalopathies, toxic conditions, infectious diseases.

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6
Q

Tics

A

Rapid, stereotyped, coordinated or patterned movements that are under partial voluntary control.

Complex tics are coordinated and sometimes including:

  • Jumping
  • Noises
  • Coprolalia
  • Lip smacking
  • Touching
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7
Q

Chorea

A

Characterized by involuntary, rapid, non-stereotypic, random, purposeless movements of body structures.

Present at rest, during sustained postures, and voluntary movement.

Causes can be:

  • Degenerative
  • Inflammatory
  • Infectious
  • In response to drugs
  • During pregnancy
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8
Q

Ballismus

A

Involves gross, abrupt contractions of axial and proximal muscles of extremities that produce wild, flailing movements.

When unilateral, the condition is called hemiballismus.

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9
Q

Athetosis

A

Characterized by slow, writhing, purposeless movements that tend to flow into one another.

Often considered a major category of cerebral palsy.

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10
Q

Dystonias

A

A collection of syndromes and physical signs characterized by involuntary abnormal postures resulting from excessive co-contraction of agonist and antagonist muscles.

Can be primary or secondary to other neurologic conditions.

Movements can be slow and sustained with quick movements superimposed occasionally.

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11
Q

Specific Dystonias

A

When only orofacial muscles are involved, it’s called Orofacial Dystonia, and can be focal or confined to a single structure.

Cervical dystonia is characterized by tonic or clonic spasms of the neck muscles, which causes deviation of the head to the left or right, or sometimes back or forward.

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12
Q

Spasm

A

Term that designates various abnormal muscular contractions.

Spasms are usually involuntary

  • Tonic Spasms are prolonged or continuous.
  • Clonic spasms are repetitive, rapid in onset, and brief.
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13
Q

Tremor

A

Most common involuntary movement.

Involves rhythmic, periodic movements of a body part.

  • Resting Tremor occurs when the body part is in repose
  • Postural Tremor occurs when the body part is maintained against gravity
  • Action Tremor occurs during movement
  • Terminal Tremor occurs as the body part nears a target.
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14
Q

Etiologies

A

Caused by any process that damages the circuitry associated with hyperkinesias.

Cause is frequently unknown but can include:

  • Degenerative
  • Toxic/Metabolic
  • Infectious
  • Vascular
  • Trauma
  • Neoplastic
  • Inflammatory
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15
Q

Degenerative Diseases

A

Chorea is the most common characteristic, along with dementia, depression, personality changes, attention deficits, dysarthria, and dysphagia.

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16
Q

Huntington’s Disease

A

An inherited autosomal dominant degenerative CNS disorder.

Onset around 35-55 typically; is fatal

Early signs:

  • Clumsiness
  • Lack of focus
  • Moodswings
  • Slight uncontrollable movements

As the disease progresses:

  • Speech difficulty; slurring of words
  • Weight loss
  • Uncontrollable movements such as jerking of face/mouth.
17
Q

Toxic/Metabolic Conditions

A

Neurometabolic disorders and drugs that affect neurotransmitter balance in the BG can cause chronic, progressive, acute, or delayed-onset involuntary movements.

18
Q

Infectious Processes

A
  • Chorea (Sydenham’s Chorea is associated with streptococcal infections)
  • Tics
  • Dystonia
  • Behavioral and emotional disturbances
19
Q

Trauma

A

Infrequent cause of movement disorders but can causally be associated with certain forms of myoclonus, tremor, and dystonias.

20
Q

Tumor

A

Tumors of the BG and thalamus have been associated with chorea and dystonia.

21
Q

Patient Perceptions

A

Patients with non-rhythmic hyperkinesias of the jaw, face, tongue, or larynx describe speech as slurred or hard to get out.

Chewing and swallowing complaints common with chorea and dystonia.

Complains of tightness and inability to move, or control movements in affected structures.

22
Q

Chorea Oral Mech: Non-Speech

A

Drooling

Swallowing difficulties

Quick, involuntary movements at rest.

23
Q

Chorea Oral Mech: Speech

A

Conversation, reading, and speech AMR are useful tasks for articulation breakdowns

Vowel prolongations permit observation of fluctuations

24
Q

Chorea: Prominent Deviant Speech Characteristics

A

Sudden, involuntary inspiration or expiration

Harsh, strained-strangled VQ, excess loudness variations

Mild hypernasality

Imprecise articulation

Monopitch, monoloudness, reduced stress, short phrases

25
Q

Action Myoclonus

A

Dysarthria is common in patients with action myoclonus in non-speech muscles.

Anoxic encephalopathy is common cause.

26
Q

Tourette’s Syndrome

A

A neurodevelopmental disorder characterized by multiple motor and 1+ vocal tics.

Emerges before 18 years.

Tics can be brief and isolated or consist of purposeful movements; sometimes include repetitive noises and sounds.

27
Q

Dystonia: Non-Speech Oral Mech

A

Drooling

Dysphagia at oral or pharyngeal phases

Complaints that food gets stuck in throat

Difficulty chewing

28
Q

Dystonia: Speech

A

Excess loudness variations

Harsh, strained-strangled voice quality; voice stoppages

Mild hypernasality

Imprecise articulation and articulatory breakdowns

Monopitch, monoloudness, short phrases, reduced stress

29
Q

Spasmodic Dysphonia

A

Uncommon voice disorders that reflect dystonic movements of laryngeal muscles triggered by speech.

Can be adductor (strained/squeezed quality), abductor (breathy), or mixed.