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phonology
sound system of a language and the rules that govern the sound combinations
when to use the ‘s’ sound and when to use the ‘z’ sound (helps vs crabs)
morphology
system that governs word structure and construction of word forms
study of stems, root, prefix (happy, unhappy, happiness)
syntax
system governing word order and combination to form sentences, and the relationships among the elements within a sentence
english: how old are you vs spanish: how many years do you have (cuantos anos tienes)
semantics
system that governs word meaning and sentences
crash can mean accident, to attend party without invitation, waves hitting shore, etc
pragmatics
system that combines all language components in functional and socially acceptable conversation
its raining cats and dogs, crack the door open
prosody
tool of human expression conveyed acoustically by way of durational, intensity, and frequency cues, planned and programmed in speech
the melody of language
receptive language
a person's ability to understand and process spoken, written, or nonverbal communication, such as gestures and visual cues
input or auditory comprehension
expressive language
the ability to put thoughts, ideas, and feelings into words or other communication forms so that other people can understand them
diagnostic classifications, general - articulation disorder
speech sound disorder w no known cause, difficulty producing speech sounds resulting in sound omissions, substitutions, or distortions of speech sounds
wed for red, nana for banana, lisp
phonological disorder
difficulty learning the sound system of a language and the rules for combining sounds
rule-based errors must affect MORE than one sound (stopping, fronting, final consonant deletion)
diagnostic classifications, general - childhood apraxia of speech (CAS)
severe speech sound disorder, inability of a person to perform voluntary/skillful movements of articulators without paralysis
characteristics of childhood apraxia of speech
Severe and persistent speech difficulty and/or unintelligibility
Vowel misarticulations; reduced production of consonants
Difficulties in sequencing the phonemes in syllables and words
Difficulties in producing volitional oral movements and movement sequences: silent periods during tries
Inconsistent timing control of nasality and prosody
Inappropriate use of prosody, especially syllable stress
diagnostic classifications, general - developmental dysarthria
Difficult or unclear articulation of speech that is otherwise linguistically normal.
Due to motor incoordination or weakness of the muscles needed to articulate intelligible speech
diagnostic classifications, general - spoken language disorder (SLD)
language disorder focusing on oral communication—specifically listening and speaking
diagnostic classifications, DSM - language disorder
Persistent difficulties in acquisition and use of language
• Reduced vocabulary
• Limited sentence structure
• Impairments in discourse
diagnostic classifications, DSM - speech sound disorder
Persistent difficulty with speech sound production which interferes with intelligibility or prevents verbal communication
Disturbance limits effective communication and interferes with social participation, academic achievement, or occupational performance
diagnostic classifications, DSM - childhood-onset fluency disorder
Disturbances in normal fluency and or timing that persist overtime and cause anxiety about speaking
Sound and syllable repetitions, Sound prolongations of consonants as well as vowels, Broken words, Circumlocutions (word substitutions to avoid problematic words), Words produced with excess physical tension, Monosyllabic whole-word repetitions
diagnostic classifications, DSM - social (pragmatic) communication disorder
Persistent difficulties in social use of verbal or non-verbal communication
difficulty using communication for social purposes, inability to change communication to match context, difficulty following rules for conversation, trouble w idioms, metaphors
speech
how we say sounds and words
those with speech problems may not say sounds clearly, repeat sounds, pause when speaking (stuttering), hoarse/ raspy voice
language
the words we use to share ideas and get what we want
those with language disorder may have trouble understanding, talking, reading, writing
speech disorders
impairment of the articulation of speech sounds, fluency and/or voice
language disorders
impaired comprehension and/or use of spoken, written, and/or other symbol systems
involves form (phonology, morphology, syntax) content (semantics) or function (pragmatics) of language
when to refer for speech/language disorders?
when a child misses key developmental milestones (such as no babbling by 12 months, no single words by 16–18 months, or speech that is mostly unintelligible) or shows regression in speech, language, or social skills at any age
when not to refer for speech/language disorders?
if speech differences are normal, developmentally appropriate, or due to an illness or infection
Who can/should be part of a multidisciplinary assessment team for speech and/or language difficulties?
SLP, pediatrician, audiologist, occupational therapist, learning specialist, psychiatrist, psychologist
common treatment approaches for language disorders
social language skills (pragmatics): staying on topic, conversational turns, recognizing and repairing breakdowns
vocabulary (semantics): vocab is taught with a developmental sequence, organization of lexicon
grammar (morphology and syntax): awareness of syllables and sounds, roots/affixes, relationships w/ other words, verbs tenses, pronouns, etc
common treatment approaches for speech disorders
motor-based approach: if articulatory based, discriminate and contrast the sounds in error, produce sounds in isolation followed by single syllables, words, phrases, and sentences, produce target sounds correctly in conversational speech
Linguistic phonological approach: used when one has inadequate knowledge of the sound system, teach phonological rules, sound contrasts, and phonological patterns of the language
eye anatomy - iris
thin, ring-shaped, colored part of the eye located between the cornea and the lens
eye anatomy - lens
transparent, biconvex structure inside the eye that helps focus light onto the retina
eye anatomy - pupil
dark, circular opening in the center of the Iris that allows light to enter the eye
eye anatomy - cornea
transparent, dome-shaped outer covering at the front of the eye
eye anatomy - retina
a thin, light-sensitive tissue lining the back wall of the eye
eye anatomy - choroid
vascular, pigmented layer of the eye located in the middle layer of the eyeball wall (the uvea)
eye anatomy - optic nerve
a sensory nerve that carries visual information from the retina to the brain
eye anatomy - optic disc
circular to vertical-oval exit point at the back of the eye where retinal ganglion cell axons bundle together to form the optic nerve.
strabismus
misalignment of the eyes (esotropia, exotropia, or vertical misalignment)
strabismus - esotropia
eye turns inward (crossed eyes)
strabismus - exotropia
eye turns outward (wall eyes)
strabismus - hypertropia
eye turns upward
strabismus - hypotropia
eye turns downward
nystagmus
back-and-forth movement of the eyes due to poor vision, neurologic conditions, or idiopathic
abnormal head posture
related to vision impairment, due to strabismus, ptosis, astigmatism, or nystagmus
abnormal color vision
related to vision impairment, seen in colorblindness (1 in 12 males) and retinal/optic nerve disorders
photophobia
related to vision impairment, an abnormal intolerance, discomfort, or eye pain caused by exposure to light
seen in infantile glaucoma, aniridia, albinism, and achromotopsia
refractive errors
The shape of your eye does not bend light correctly, resulting in a blurred image (3 main: myopia, hyperopia, astigmatism)
refractive errors - myopia
nearsightedness, difficulty seeing far
refractive errors - hyperopia
farsightedness, difficulty seeing close
refractive errors - astigmatism
irregular curve in cornea or eye lens
refractive correction - myopia
eyeball too long = concave lense deflects rays
refractive correction - hyperopia (farsightedness)
eyeball too short = convex lens
refractive correction - astigmatism
eyeball correct size, cornea misshaped = cylindrical lens
amblyopia
lazy eye, happens in just 1 eye, breakdown in brain + eye teamwork, brain can’t recognize sight from 1 eye
starts in childhood, most common cause of vision loss in kids
refractive errors, cataracts, strabismus can lead to lazy eye
cerebral visual impairment (CVI)
Visual deficit due to disorders affecting the visual cortex
Ocular exam can be normal
ranges from mildly impaired to completely absent
Causes due to hypoxic ischemic encephalopathy, CNS malformations, neoplasia, infection, metabolic neurodegenerative disorders, underlying genetic causes
Vision may improve with time
optic nerve hypoplasia
disorder from birth, underdevelopment of optic nerve
most have abnormal eye movements (nystagmus), vision ranges from no light to functional vision or full vision in one eye
uncorrectable with glasses
may be associated with pituitary abnormalities
associated with other disabilities
optic nerve atrophy
interferes with optic nerve’s ability to transmit impulses
caused by tumor, glaucoma, etc
symptoms: blurred vision, trouble w/ peripherials and colors, reduction in sharpness
retinopathy of prematurity (ROP)
Abnormal vessel growth leading to tractional retinal detachment if untreated.
Vision loss due to high refractive error or retinal damage
treated with retinal laser, surgery, anti-VEGF injections
chorioretinitis
inflammation of the choroid, which is a lining of the retina deep in the eye
can be cased by infection or autoimmune disease
symptoms may not appear for 10-20 years
symptoms: pain, redness, blurred vision, floating objects, light sensitivity, glare, tearing, sparks/flashes, impaired night + color vision, distortion of objects
cataract
defect in lens clarity, appearing as white spot on pupil, can require surgery
blindness
Corrected visual acuity of 20/200 or worse in the better eye, and/or a limited visual field of 20 degrees or less
low vision
corrected vision of 20/70 to 20/200
causes of blindness
cerebral visual impairment
optic nerve hypoplasia
inherited retinal disorders
retinopathy of prematurity
cataract
glaucoma
poor nutrition
infection
microphthalmia
birth defect in which one or both eyes did not develop fully, so they are small
1 in 5200 babies, causes unknown
charge syndrome prevalence
8500 to 10000 newborns
anophthalmia
birth defect where baby is born without one/both eyes
CHARGE syndrome
Coloboma of the eye
Heart defect from birth
choanal Atresia
Retarded growth/development
Genital abnormalities
Ear marformations (w/ or w/out hearing loss)
CHARGE syndrome - coloboma
gap or hole in one of the structures of the eye, forms during early development
present in one or both eyes
treatment for visual impairment - refractive error correction
glasses: may need atropine drops, straps, tinted lenses, special frames
contact lens: used in high hyperopia and anirdia
refractive surgery if glasses not tolerated
treatment for visual impairment - amblyopia
refractive error correction, eye patching, atropine eye drops, penalization of better eye, surgery
works well, usually prevents long-term vision problems
not effective after first decade of life
treatment for visual impairment - ophthalmic surgeries
catract removal, strabismus repair, glaucoma surgery, ptosis repair, retinal surgery
in some cases, surgery must be done in infancy for vision to develop properly
causes of visual impairments
ocular
light must pass clearly through cornea → lens → vitreous and strike a functioning retina in order to see
optic nerve
connects the eye to the brain, any nerve damage decreases vision
cortical/cerebral
occipital lobe in the posterier brain = visual processing center, damage results in poor vision
interventions for visual impairments
clinical, rehabilitation, educational
increases skills in other senses, improves body concept and awareness, promote locomotion and environmental exploration
home based sessions/school based preschool programs
optical aids and devices, braille, computers, audio/orientaiton/mobility techliques
assistive tech, voice recognition, global positioning
genetic advances (gene replacement)
impact of visual impairment on development - motor
abnormal movements, hands fisted longer, head lower, crawling + standing + walking at a later age, fine motor skills / balance affected, decreased mobility = obesity
impact of visual impairment on development - language
imitates sounds earlier, less facial/body language, fewer questions, delay in combining words, difficulties with pronouns, less adjectives
impact of visual impairment on development - psychosocial
poor eye contact impacts attachment and socialization, isolation, poor-self image, higher rates of mental health issues
ear anatomy - pinna (or auricle)
the visible, outer portion of the ear that projects from the side of the head

ear anatomy - ear canal
s-shaped tube that connects the outer ear (pinna/auricle) to the eardrum

ear anatomy - malleus
hammer-shaped bone in the middle ear

ear anatomy - incus
middle bone of the small auditory ossicles in the middle ear

ear anatomy - stapes
smallest and lightest bone in human body, serves as the innmost middle ear ossicle

ossicles
the three smallest bones in the human body, located inside the middle ear, which transmit and amplify sound vibrations from the eardrum to the inner ear
ear anatomy - tympanic membrane (eardrum)
thin, cone-shaped tissue that separates the outer ear canal from the middle ear, vibrates when sound waves hit

ear anatomy - cochlea
snail shell-shaped, fluid-filled organ in the inner ear that turns sound waves into electrical signals for the brain

ear anatomy - labyrinth
complex system located deep within the petrous part of the temporal bone, responsible for both hearing and balance

ear anatomy - auditory nerve
sensory nerve that transmits sound signals from the inner ear to the brain

1-3-6 guidelines
hearing screening by 1 month
diagnosis by 3 months
intervention by 6 months
critical window for language development
early identification → early intervention → supports language development
diagnostic overshadowing - underdiagnosis
Incorrectly attributing hearing loss as the reason for a developmental difference
Lack of diagnosis often translates into a lack of early intervention, which can impact long-term outcomes
Child and family misses out on appropriate services
diagnostic overshadowing - overdiagnosis
Incorrectly attributing to a developmental disability
Supports and intervention, if not appropriate, may not help needs nor prepare families
Schools and programs may not accept the child
interventions - language learning
auditory-oral: no sign, use residual hearing
auditory-verbal: hearing aids or implants, play-based
cued speech: sign and mouth movements
sign supported speech: sign and speech
ASL: sign only
interventions - amplification
hearing aid or cochlear implant
types of hearing loss - sensorineural
inner ear, caused by damage to hair cells of spiral ganglion neurons of cochlea
sound cant be converted into signals
often permanent
treatment for sensorineural hearing loss
amplification via hearing aids or cochlear implants
types of hearing loss - conductive
outer or middle ear, sound waves cant go thru outer ear canal to eardrum
reduction in sound levels
can be corrected surgically/medically
bone conduciton hearing aids
types of hearing loss - combine or mixed
combination of sensorineural and conductive
problems transmitting sound thru outer/middle ear, reduced cochlear function
conductive may be treated, sensorineural often permanent
treatment: hearing aids (unless infection)
types of hearing loss - neural hearing disorders
auditory nerve, sound processed by inner ear but signal transmission to brain is impaired
trouble w/ speech perception
audiogram
frequency/pitch (Hz) = x axis
intensity/amplitude/loudness (dB) = y axis
types of hearing screeners - auditory brainstem response (ABR)
tests how inner ear and brain pathways work
used for kids who cant complete typical hearing screening
used if symptoms are due to hearing loss in the brain/brain pathway
test done at rest, no verbal responses needed
types of hearing screeners - otoacoustic emissions (OAE)
used to find out how well inner ear works
measures otoacoustic emissions (sounds given off by inner ear when responding to a sound)
hair cells in inner ear vibrate
types of hearing screeners - pure tone testing
pitch - most humans can hear from 20-20,000 Hz
risk factors for D/HH children
neonatal factors
prematurity
intraventricular hemorrhage
necrotizing enterocolitis (NEC)
prolonged ventilation
bacterial meningitis
some genetic syndromes
family history of learning disabilities or attention problems
causes of hearing loss - genetic
1 in 2 cases of hearing loss, 80% autosomal recessive
feature of many syndromes: treacher collins, waardenburg, bardet-biedi, usher, down, trisomy 13, trisomy 18
commmon non syndromic - mutation on connexin 26