Module 2 Flashcards
Overview of Early Comm. Impairments:
developmental disabilities
about… children aged 3-17 were diagnosed with DD
Some groups of children more likely to be diagnosed:
- more ?
-…. children
children living in
children with
1/6 (17%)
boys compared to girls
non-hispanic white and non-hispanic black children
rural areas
public health insurance
Communication Impairment:
refers to difficulty ? in … or .. communication
a comm. impairment may:
affect
range in severity from
be … or ..
receiving, sending, processing and comprehending concepts / verbal or nonverbal
hearing, language or speech
mild to profound
dev. or acquired
Risk of Comm. Impairment:
…factors
biological: …
environmental:
-…status
parental
poor
poor access to
…
biological and environmental factors
genetic or gestational disorders, prematurity, LBW
socioeconomic status
parental mental illness
nutrition
healthcare
abuse
Communication Impairment runs in ?
approximately half of children with comm. impairment have a ?
families
person in their family also affected
Young children who are ELL do not ? however dual language learners with diff. in acquisition of their ? may be eligible
qualify
native language and second language
Intellectual disability:
impairment in ability to ?
diagnosed by IQ of less than impacting
Causes of ID are ?
think, reason, learn
70/ adaptive function in conceptual, social, practical domains
diverse and may be unknown
Developmental Disability:
umbrella terms that covers disorders that appear
intellectual disability is an example of one ? BUT can occur outside of ?
during developmental period
dev. disability / developmental period
Chromosomal disorders
can be due to:
errors in
chromosome
chromosomal ?
number of chromosomes
deletions
defects
Fragile X:
leading ?
caused by mutation on
deficits:
can occur in ? but more severe in ?
biological cause of ID in infants
X chromosome
reciprocity, play skills, gestures, relative strength in vocal comm.
females/ males
Down SYndrome:
caused by additional >
deficits include ? that is more severe than ?
order or progression of language skills similar to typical children but?
genetic material on 21st
language delay/cognitive delay
SLOWER
Prader-Willi Syndrome:
rare genetic disorder caused by gene deletion on ?
majority have
40% have mild
deficits:
-low
-short
-…disability
-..behavior
-incomplete
-chronic feelings of ?
linguistic. deficits:
poor
shorter
poor
poor …skills
gene deletion on chromosome 15
ID
mild ID
low muscle tone
short stature
cognitive disability
problem behavior
incomplete sexual development
chronic feelings of hunger
phonological skills
shorter utterances
poor narrative skills
poor oral motor skills
ASD neurodevelopmental disorder
social…
…,.. behaviors
present during ? but not fully manifested until
can be formally diagnosed … months, but routinely not being diagnosed until ?
comm. often primary ? with … percent remaining nonverbal
causes varied by … link on chromosome X
structure and neurological function different in
comm. problems
repetitive, restrictive behaviors
early dev./ laater
warning signs early as 9 months/ 18-24 months/ 4 or 5 years
area of concern/ 20-30%
genetic
brain of children with ASD
CP: most common cause of severe
non-progressive motor disorder as a result of ?
damage occurs? but may occur?
characterized by disturbances in ?
-
-
-
-
often accompanied by other ? secondary to muscoskeletal problems
motor impairment in children
static or permanent injury to fetal developing brain
in utero/ around time of birth
movement and posture
-spasticity (spastic)
-involuntary movement (dyskinetic)
-shaky moverment (ataxic)
mixed
neurodevelopmental disorders or impairments
CP:
Speech and Lang. difficulties include
-difficulty
…
…language delay
overwhelming majority diagnosed with CP will also have ?
85% of children with CP between 24-39 months of age - 3 groups identified
44% not
41% emerging
15% established
difficulty swallowing
dysarthria
receptive/expressive language delay
speech and lang. impairments which persist into school-age years
yet talking
emerging talkers
established talkers
Sensory disorders:
deafness:
threshold… or more
functional deafness: person relies on vision for
most common cause is genetic in form of
most hearing impairment occurs in hearing families but impact on language is less in families that ?
90db or more
environmental info and learning lang.
recessive gene
impact on language is less in families that sign for children pre-ling. deafness