Motor Speech Disorders: Anatomy, Signs, and Treatment Strategies

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41 Terms

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Primary motor cortex

Precentral gyrus — Betz cells

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Lower motor neurons (LMNs) for cranial nerves

Brainstem cranial nerve nuclei

Spinal cord anterior horn cells

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Classic hallmark sign of an LMN lesion affecting speech muscles

Atrophy and fasciculations in the affected muscles

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Characteristic sign of an UMN lesion

Spasticity, hyperreflexia, and Babinski sign

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Extrapyramidal (indirect activation) system contribution

Regulation of tone, posture, and reflexive adjustments that support movement

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Lower facial weakness affecting the entire ipsilateral face

Ipsilateral LMN lesion (facial nerve nucleus or peripheral nerve)

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Contralateral weakness only of the lower quadrant of the face

Contralateral UMN (supranuclear) lesion affecting corticobulbar fibers

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  • basal ganglia damage

  • associated with Parkinson's disease

Hypokinetic dysarthria

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Patient presentation with slow, effortful, strained voice

Reduced pitch variability, hypernasality, and slow rate

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Spastic dysarthria

Which dysarthria type is most likely?

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Respiration, phonation, resonance, articulation, and prosody

Which subsystem(s) of speech are evaluated in a comprehensive motor speech examination?

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Isolated reading of a single word list with no connected speech sample or nonspeech tasks

Which of the following is LEAST useful for differential diagnosis of dysarthria?

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Hypokinetic dysarthria (Parkinson disease)

Lee Silverman Voice Treatment (LSVT LOUD) is an evidence-based treatment most often used for which motor speech disorder?

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Activity and participation

Which ICF domain addresses how a speech impairment affects daily life activities and social roles?

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Nonmaleficence

In motor speech counseling, which of the following ethical principles requires that clinicians do no harm and avoid interventions likely to cause damage?

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Irregular articulatory breakdowns and prosodic excess (scanning speech)

A hallmark sign of ataxic dysarthria is:

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Developmental norms, family involvement, and neuroplasticity considerations

When evaluating a pediatric client with suspected motor speech disorder, clinicians must first consider:

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Intention tremor and ataxic gait

A lesion of the cerebellum is most likely to produce which non-speech motor sign?

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Bilateral UMN (pyramidal) lesions or bilateral cortical involvement

Pseudobulbar affect (involuntary laughing/crying) is most commonly associated with:

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Nasal emission on consonants and hypernasality on vowels

Which clinical measure is most specific for identifying velopharyngeal incompetence during speech?

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Assessing language and literacy, family roles, beliefs about disability, and adapting interventions accordingly

Cultural competence in motor speech practice should include:

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Muscle atrophy in affected muscles; Breathiness and reduced voice loudness; Fasciculations

Features commonly seen with flaccid dysarthria (select all that apply)

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Oral mechanism exam including cranial nerve assessment; Perceptual speech tasks (AMR/SMR, connected speech, reading); Review of medical history and neuroimaging (if available)

Components of a thorough motor speech evaluation include (select all that apply)

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Bradykinesia and reduced amplitude of movement; Resting tremor and rigidity; Chorea or dyskinesias

Clinical signs that point toward a basal ganglia (extrapyramidal) disorder include (select all that apply)

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Rate control strategies and pacing boards for ataxic dysarthria; LSVT LOUD for hypokinetic dysarthria; Use of AAC when severity prevents functional communication

Evidence-based interventions for motor speech disorders can include (select all that apply)

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Forehead involvement spared (suggests UMN); Presence of fasciculations in facial muscles (suggests LMN); Weakness affects both upper and lower face on same side (suggests LMN)

When making a differential diagnosis between UMN and LMN facial weakness, useful clues include (select all that apply)

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Obtaining informed consent; Balancing patient autonomy with clinician recommendations; Discussing realistic goals and prognosis with families

Important ethical considerations when working with clients with motor speech disorders include (select all that apply)

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Respiration; Phonation; Resonance

The five speech subsystems where signs of dysarthria are observed include (select all that apply)

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Stage of grief; Health literacy and cultural beliefs; Providing resources, AAC options, and referrals

Factors that should be considered in counseling families of individuals with motor speech disorders include (select all that apply)

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Ipsilateral cranial/spinal nerve motor neuron cell bodies and peripheral nerves terminating in muscle

Final common pathway

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Corticospinal / corticobulbar fibers originating in motor cortex for skilled voluntary movement

Direct activation pathway (pyramidal tract) — primary clinical function

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Regulation of movement, muscle tone, and involuntary movements (basal ganglia influence)

Indirect activation pathway (extrapyramidal system) — primary clinical function

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Brainstem or peripheral nerve nucleus/axon lesion (e.g., CN VII nucleus or nerve) — weakness, atrophy, fasciculations

Flaccid dysarthria — typical lesion location

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Bilateral UMN (corticobulbar) lesions — spasticity, slow strained voice, hypernasality

Spastic dysarthria — typical lesion location

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Cerebellum (coordination) — irregular articulation, prosodic disturbances

Ataxic dysarthria — typical lesion location

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Reduced loudness and monopitch; masked facies (e.g., Parkinsonism)

Hypokinetic dysarthria — common coexisting non-speech sign

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Involuntary movements (e.g., chorea, dystonia) and variable articulatory breakdowns

Hyperkinetic dysarthria — common perceptual speech sign

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Measurement of respiratory-phonatory support and breath control for speech

Maximum phonation time (MPT) — what it primarily assesses

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Family support, communication partner training, or workplace adaptation

An important ICF environmental factor for motor speech treatment

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Bilateral corticobulbar damage producing pseudobulbar signs (e.g., severe dysphagia, emotional lability)

A clinical sign suggesting bilateral UMN involvement rather than unilateral UMN

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Device/strategies to support participation when natural speech is insufficient

AAC (augmentative and alternative communication) — role in motor speech management