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Childhood Motor Speech Disorders

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tries to assist in sit but lacks head control; back still rounded ... head maintained in midline and aligned with trunk in supported sitting ... – PowerPoint PPT presentation

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Title: Childhood Motor Speech Disorders


1
Childhood Motor Speech Disorders
  • Julie M. Liss, Ph.D.
  • SHS 567

2
Childhood vs. Adult MSD
  • How does speech production (and language) develop
    in a physically impaired system?
  • Localization is not so neat with kids.
    Classification is difficult
  • Consider language, cognition, perception,
    feeding, and speech in kids.
  • Many disorders stem from no obvious lesion.

3
Where do we see childhood MSD?
  • Schools
  • hospitals
  • private practice

4
Our Role
  • Diagnose if possible
  • Treat, usually as part of a multidisciplinary
    approach
  • Aim for maximum level of communication with least
    effort (verbal/vocal )

5
Taste of the Controversy
  • Speech--feeding relationship
  • early intervention efficacy
  • oral motor exercises
  • drooling therapy
  • biofeedback technology
  • AAC

6
Diagnostic Controversy...
  • Does Developmental Apraxia of Speech exist?
  • What does it look like?
  • Why does it occur?
  • Do we treat it differently than other speech
    disorders in childhood?

7
What Constitutes Normal
  • Before discussing diagnosis of motor speech
    disorders, lets examine normal development...

8
Prespeech Assessment
  • General Observations
  • oral motor control
  • gross and fine motor control
  • Specific prespeech functions
  • articulator assessment
  • feeding assessment (nursing, transitional,
    modified adult form)
  • vocalization assessment

9
Motor Development Milestones
  • Neonate (0-10 days)
  • physiologic flexion
  • reflexes prominent and strong
  • prone head slightly to one side pelvis high
  • supine head at 45 degrees to side flexor recoil
    of upper and lower extremities hand loosely
    fisted
  • sitting no flexor control head lag and flop
    back rounded

10
Milestones Continued...
  • 1 Month
  • decreased flexion throughout
  • head lifting begins
  • random extremity movements
  • reflexes remain prominent and strong
  • sitting makes fleeting attempts to control head
  • smiles can visually fixate

11
Milestones continued...
  • 2 Months
  • asymmetry prominent
  • obligatory ATNR prominent
  • decreased hip flexion
  • tries to assist in sit but lacks head control
    back still rounded
  • more smiles visual tracking begins

12
Milestones continued...
  • 3-4 Months
  • beginning of symmetry
  • head maintained in midline and aligned with trunk
    in supported sitting
  • visual recognition of parents smiling laughing

13
Milestones continued...
  • 5-9 Months
  • independent sitting and crawling begins
  • primitive reflexes diminish and disappear
  • trunk lateralization in sitting, standing,
    crawling
  • visual interest in small objects stranger
    anxiety
  • begins transitional stage of swallow

14
Milestones continued...
  • 10-18 Months
  • trunk stability and refinement of upper extremity
    coordination
  • walking with, then without support pinching
    grasp transfers object from hand to hand
  • first words and phrases appear
  • begins modified adult pattern of eating

15
Normal Infant Oral Reflexes Present at Term
  • Gag
  • phasic bite
  • tongue thrust
  • rooting
  • suckling
  • Babinski
  • ATNR

16
Abnormal Movements and Reflexes not seen in the
Developing Infant
  • Jaw thrust
  • tonic bite
  • lip retraction/pucker
  • tongue retraction
  • jaw clenching

17
Assessment and Classification of MSD in Children
  • Sensorimotor Programming
  • DAS
  • Neuromotor Execution
  • UMN Spastic CP
  • UMN BG Dyskinetic CP
  • UMN CBM Ataxic CP
  • UMN meningitis, TBI

18
Classification continued...
  • LMN
  • motor nuclei Moebius syndrome
  • axons of cranial or spinal nerves Guillain-Barre
  • neuromuscular junction myasthenia gravis
  • muscle fibers muscular dystrophy

19
DAS
  • No known lesion or etiology
  • neurologic soft signs language deficits oral or
    other apraxia
  • awkward groping movements inconsistent
    articulatory errors syllable sequencing errors
    consonant and vowel distortions, substitutions,
    omissions hypernasality

20
The Disagreements
  • Etiology and pathology
  • Signs, symptoms, or syndrome?
  • The symptoms themselves

21
UMN Spastic CP
  • Hemiplegia paraplegia diplegia quadriplegia
  • spastic dysarthria, dysphagia, especially with
    spastic quadriplegia decreased respiratory
    support breathy, strained strangled voice
    monopitch and loudness
  • disturbances in cognition, perception, sensation,
    language, hearing, emotions, behavior, feeding
    seizures common

22
UMN BG Dyskinetic CP
  • Hyperkinetic dysarthria rapid, irregular
    breathing forced voice quality with weak
    intensity large jaw movements with gross tongue
    positioning unstable velum
  • motor development slow failure to sit
    dysphagia cognitive deficits

23
UMN CBM ataxic CP
  • Ataxic dysarthria irregular articulatory
    breakdown errors of voicing inappropriate
    variation of pitch and loudness equal and even
    stress possible
  • dyssynergia wide-based gait action tremor,
    hypotonia dysmetria nystagmus

24
UMN Meningitis, TBI
  • Spastic or mixed dysarthria
  • profile varies with etiology

25
LMN motor nuclei
  • Flaccid dysarthria primarily articulation
    deficits secondary to facial or other paralysis
  • in Moebius syndrome congenital bilateral CN VII
    paralysis feeding problems hearing loss
    language delays mental retardation

26
LMN axons
  • Flaccid dysarthria respiratory, phonatory,
    articulatory, resonance deficits possible speech
    may be severely affected, prohibiting oral
    communication
  • Guillain-Barre symmetrical muscle paralysis
    following infection (CN VII, IX, X) dysphagia
    prognosis often good

27
LMN neuromuscular junction
  • Flaccid dysarthria hypernasality that worsens
    with fatigue
  • myasthenia gravis classic symptom is muscle
    weakness after sustained contraction
    hypernasality secondary to CN X involvement
    ptosis dysphagia respiratory deficits

28
LMN muscle fibers
  • Flaccid dysarthria not common in the MD
    population may be very mild articulatory,
    phonatory, and respiratory deficits until late in
    the disease when alternative forms of
    communication are required
  • X-linked inheritance onset between 2-5 years of
    age affects pelvis and trunk before limbs and
    head

29
DIAGNOSTIC SUMMARY
  • Differential dx difficult and not necessary in
    kids (especially young ones)
  • primary goal is to determine best modes of
    communication in short and long term
  • think functional--think whole kid

30
Video Handling Children with tone problems
31
Continua of Sensory Input
  • Rhythm slow -- fast
  • Pressure firm -- light
  • Reps consistent -- intermittent
  • nature palm -- finger pads
  • area proximal -- distal
  • orientation midline -- lateral
  • mouth closed -- open
  • effects calming -- stimulating
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