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Developmental disorders
become evident as a baby or child develops, often without na clear cause
Congenital disorders
present at birth (e.g., down syndrome)
Acquired disorders
emerge in a person who previously had typical communication, often due to an illness or neurological event (e.g., stroke)
Functional
no known cause
Articulation
motor aspects
Phonology
linguistic aspects
Organic
developmental or acquired
Motor/neurological
Execution (dysarthria), Planning (apraxia)
Structural
Cleft palate/other orofacial anomalies, Structural deficits due to trauma or surgery
Sensory/perceptual
hearing impairment
Structural causes of speech sound disorders
Imprecise articulation due to structural damage or abnormality of the articulators
Cleft palate
Failure of the lip and/or the palate to fuse during fetal development, A congenital condition, Makes it difficult or impossible to speak typically, Can be repaired surgically, but speech sound disorder may persist
Cleft lip
problems with labial sounds
Cleft palate
hypernasality, incomplete constriction of oral cavity
Neuromotor causes of speech sound disorders
Imprecises articulation due to impaired nervous system control of the muscles (dysarthria, apraxia of speech
Dysarthria
muscles are weak or paralyzed, lack coordination, or a combination of the above
Apraxia of speech
problems with planning how to move the muscles
features of dysarthria
Imprecise articulation, Speech is slow and effortful, Disorders of voice and/or respiration are common
causes of dysarthria
congenital, acquired neurological conditions (stroke, parkinsons disease, amyotrophic lateral sclerosis (ALS)
Apraxia of speech
No muscular weakness or paralysis
features of apraxia of speech
Imprecise articulation, Speech is slow and effortful, May struggle with the articulators (“articulatory groping”), Disorders of voice or respiration are not common
causes of apraxia of speech
Developmental disorder in children, Acquired disorder in adults, often resulting from stroke
Classifying Articulation and Phonological Errors
Speech rate and rhythm is normal, No problems with voice and respiration
Articulation
Decrease in accuracy of articulation as a result of incorrect placement or movement of articulators
types of speech disorders
Typical developmental (before school age) and phonological speech sound disorders (school age and older), Structural and neuromotor speech sound disorders
Typical developmental (before school age) and phonological speech sound disorders (school age and older)
Substitutions (I tee the wabbit—> I see the rabbit), Omissions (boo—> book)
Structural and neuromotor speech sound disorders
Distortions, Additions (galass—> glass)
Types of deletion
Final consonant deletion (bat—> ba)
Unstressed syllable deletion (above—> –bove)
Cluster reduction (step—> –tep)
Types of substitution
Assimilation, Substitution
Assimilation
Regressive (backward) assimilation (dig—>gig), Progressive (forward) assimilation (toad—>toat)
Substitution
Stopping— stop sounds are substituted for fricative (sheep—> teep), Fronting— alveolar sounds are substituted for palatal and velar sounds (came—> tame)
Assessment
identification of the child’s needs and strengths (Hearing test, Oral mechanism evaluation: structure and function, Articulation inventory and phonological processes)
Intervention methods for speech sound production in children
acquisition, generalization
Acquisition
learning to produce the sound
Minimal pairs: communicative significance
Visual cue: e.g., looking in the mirror
Tactile cues, e.g., touching the lips or throat
generalization
using the sound in new contexts
In other contexts (can—> back)
Longer utterances (words—> phrases —-> sentences)
In other context (therapy —> class activities)
With other people (clinician —> parents, peers, strangers)
voice disorders
vocal quality, volume, pitch, nasality (“resonance”), vocal fatigue, loss of voice
Voice problems
very common and usually go away quickly on their own
voice disorders
last longer and can benefit from help from a/an…
Otolaryntologist (ear, nose, and throat doctor)
Speech-language pathologist
causes of voice disorders
functional, structural, neuromotor
Functional
inefficient use of the vocal mechanisms when physical structures are normal
Structural
damage to the vocal folds
Neuromotor
paralysis or malfunction of the vocal folds due to neurological injury or disease
Visualizing vocal fold health
Acoustic measurements of the voice
Videoendoscopy
Through the mouth: rigid endoscopy, Through the nose: flexible endoscopy
rigid endoscopy
Through the mouth
flexible endoscopy
Through the nose
Functional causes of voice disorders
Inefficient use of vocal mechanism, using compensatory muscles and excessive vocal force
Muscle tension
Diplophonia
Ventricular phonation
Can lead to structural damage
Muscle Tension
Soft volume phonotation
Loud volume phonotation
Damage to the vocal folds
Swollen and irritated, due to overuse or disease
Benign growths on the larynx
Vocal nodules (small bumps)
Laryngeal cancer
Tumor
Treatment sometimes requires removal of larynx
Vocal nodules
Small bumps
Caused by overuse of the voice
Most common in young and middle-aged women (20-50)
Can cause a range of voice problems
Treatment of damage to the vocal cords
Management of use of voice
Rest the voice
Avoid yelling, coughing, etc.
Learn to project in a way that’s easier on the voice
Lifestyle changes (diet, stress)
Surgery (in some cases)
Neuromotor causes of voice disorders
Stroke or neurological disease (e.g., Parkinson’s disease, amyotrophic lateral sclerosis)
Often accompanied by dysarthria
Voice-specific neurological disorders, involving paralysis or spasms of the vocal folds
Electrolarynx
used by people who have no larynx or are unable to use the larynx to speak
Speech therapy and gender identity
Speech-language pathologists work with people to help their voice align with their gender identity
Can involve changing pitch and resonance
Dysphagia (difficulty swallowing)
Mostly affects older adults
Speech-language pathologists treat dysphagia
Swallowing and speech involve many of the same structures
Oral mechanism (mouth and tongue)
Larynx
Neural systems (e.g., cranial nerves)
Many disorders involve both speech and swallowing problems
How swallowing works
oral preparatory
oral transport
pharyngeal
esophageal
Oral preparatory
Chew food
Gather food/liquid into a “bolus” on tongue
Oral transport
Tongue pushes bolus into back of throat (pharynx)
Pharyngeal
Pharynx contracts to push bolus to esophagus
Larynx raises to protect the airway (trachea)
Esophageal
Esophagus contracts to push food into stomach
Aspiration
Refers to entry of food or liquid into the airway
Problems with third (pharyngeal) swallowing stage
Usually causes choking
If laryngeal muscles are weak, the patient may not choke (“silent aspiration”)
Frequent aspiration can cause pneumonia, a major health risk for people with dysphagia
Causes of Dysphagia
Neuromotor, Structural abnormalities or damage to the structures supporting swallowing
Assessing swallowing
Patient report of difficulties
What happens? How often? What types of foods/liquids?
Bedside testing
Typically, a screening
Yale Swallowing Protocol
Modified barium swallow
Way of visualizing the swallowing process and identifying causes of aspiration
Patient swallows liquid/food of varying consistencies, containing barium
Dysphagia treatment
Often involves otolaryngologist (ear-nose-throat doctor and speech-language pathologist
Interventions led by speech-language pathologist:
Changing posture (e.g., chin down)
Changing diet (e.g., only eating smooth foods like applesauce and soup)
Altering the consistency of food or liquid (e.g., thickening liquids)
Exercises to strengthen swallowing muscles
Medical interventions
Medications, e.g., to address reflux
Surgery to address structural problems
Stuttering
Persistent and frequent disfluencies
Impacts roughly 3 million people
Affects all ages; but typically starts between 2 to 6 years old
Can vary throughout someone’s day
Boys are 2-3x more likely to stutter compared to girls
Gender difference increases as they age: boys 3-4x more likely to stutter
Causes of Stuttering
Developmental stuttering
Many theories; different levels of explanation
Genetic
Neurological features
Brain function: more right hemisphere activation (vs. normal fluency)
Brain structure: differences in white matter pathways (vs. normal fluency)
Less efficient auditory feedback
Acquired stuttering
Neurological event (e.g., stroke, toxin exposure)
Psychogenic
Physical Signs of Struggle during Stuttering
Eye blinking
Mouth movements
Facial movements
Body or limb movements
Vocalizations
Stuttering Treatment
Direct methods: train fluency directly
Modifying stuttering: stutter more effectively
Help the client stutter more fluently with less effort
Improve the person's attitude toward stuttering
Reduce struggle and avoidance
Reduce secondary stuttering behaviors
Modifying speech: speak fluently
Slow down, change the prosody, prolong vowels
Indirect methods: trying to promote fluency without directly teaching the client how to be “fluent”
Slowing your speech rate (vs. the person who stutters)
Praising fluent speech; drawing attention to disfluent speech (children)
Delayed auditory feedback
Psychological
The auditory experience of hearing “what we hear”
Definition of sound: the disturbance of molecules within an elastic medium
This disturbance can be physically measured
Consider: properties of the source, the sound itself, and the medium
Types of Waves
Transverse
Longitudinal
Sound Waves
Initial disturbance sets vibrating molecules into motion: molecular disturbance
Sound Sources and Mediums
Depending on the elastic properties of mediums, the sound characteristics will be different
The Outer Ear
Helix
Tragus
Concha
Anti-tragus
Lobe
Out Ear Function
Outer ear resonance
Concha bowl of the pinna has a resonance of 6-8 dB around 4-5 kHz
Pinna effect has a resonance at 2 kHz and above and can vary from 3-8 dB
This is important for hearing aids
The location of the hearing aid microphone may or may not be able to take advantage of these effects
Microphone Location Effects
Graph from Chasin (1997) shows the amount of gain due to the pinna effect at the microphone for three styles of hearing aids
Note that the BTE is not able to take advantage of any of the pinna effects as its mic is located above the pinna
External Auditory Canal
Roughly 25 mm in length
Outer opening 8-10 mm
Decreases 5-6 mm in the deeper portions
Enlarges again when reaching the tympanic membrane
Outer third of the canal is cartilaginous
Inner ⅔ of the canal is bony
The Tympanic Membrane
Physical characteristics
.6 mm in thickness and 8-10 mm in diameter
Angle of 45 degrees
Conical in shape
Composed of three layers
Outer: keratinized epithelium
Middle: fibrous (lamina propria)
Inner: mucosal layer
Attached to the manubrium in the malleus
The Middle Ear
Tympanic membrane
Ossicular chain
Malleus
Tensor tympani (V)
Incus
Stapes
Stapedial muscle (VII)
Oval window
The Middle Ear
Malleus
Incus
Stapes
Tympanic membrane
The Middle Ear Function
Mechanical purpose
Transform acoustical energy into an effective and efficient means of driving the fluid of the inner ear
Increases the effective pressure of the sound energy striking the oval window
Accomplished by
Great difference between the area of the tympanic membrane (60 mm2) and the stapes footplate (3.2 mm2), and because the malleus and incus combine to form a lever
Inner Ear
Hearing and balance
Semicircular canals (balance system of the inner ear)
Vestibular nerve (balance)
CN VII
Cochlea
Cochlear nerve (hearing)=
Cochlea (latin: snail)
Tube coiled around a central axis
Modiolus
2 ½ turns in humans
30 mm in length
Three compartments or scalae
Scala vestibuli
Scala media
Scala tympani
Scala vestibuli
Above the scala media
Bounded by Reissner's membrane
Oval window opens into vestibule
Scala tympani
Below the scala media
Bounded by the basilar membrane
Round window opens into the scala tympani at the beginning of the basal turn
Scala vestibuli and tympani
Contain perilymph
Low K+ concentration, high Na+ concentration
Connected through the helicotrema
Scala media
Contains endolymph
High K+ concentration
Low Na+ concentration
Organ of Corti
Rests on basilar membrane
Basilar membrane
Series of linked resonators (turning forks!)
Stiffness varies from base to apex
Stiffer at the base than the apex
One octave every 3 mm
Double of frequency
Width increases from 0.12 mm at the base to 0.5 mm at the apex
Inner hair cells
3500 in humans
Tips do not touch the tectorial membrane
Outer hair cells
12000 in humans
Tips are strongly embedded in the tectorial membrane
Electromotile
Inner and outer hair cells
They and supporting cells form ionic barrier called reticular lamina
Separating endolymph from perilymph in tunnel of corti and surrounding areas
Cochlear Mechanics
Fluids in the inner ear are incompressible
Pressure fluctuations in the fluids occur almost instantaneously along the entire length of the cochlea
The mechanical impedance of the cochlea varies from base to apex