Please enable JavaScript.
Coggle requires JavaScript to display documents.
NEURODEVELOPMENTAL DISORDER, Genetic and neurobiological contributions,…
NEURODEVELOPMENTAL DISORDER
ATTENTION DEFICIT HYPERACTIVITY DISORDER (ADHD)
Central features
inattention, overactivity,
and impulsivity
numerous impairments
behavioral
cognitive
Social and academic problems
DSM-5 symptom types
inattentive presentation
hyperactive/impulsive presentation
Combined presentation
Facts and Statistics
Prevalence
5% of school-aged children
most commonly diagnosed in the United States
11% of children labeled with ADHD in
2011-2012
5-9% meet criteria including adults
the estimated prevalence of childhood ADHD is 5.29%
Boys are three to four times more likely to be
diagnosed with ADHD than girls.
Course of ADHD
Symptoms usually appear around age 3-4
Half of children with ADHD continue to have difficulties as adults
Impulsivity decreases, but inattention remains
Gender differences
Causes of ADHD
Biological Contributions
Genetic contributions
run in families
mutations occur - create extra copies of a gene or deletion of genes (CNVs)
Norepinephrine, GABA and serotonin also implicated
Neurobiological correlates of ADHD
Smaller brain volume
Inactivity of the frontal cortex and basal ganglia
Abnormal frontal lobe development and functioning
masalah working memory
The role of toxins
Food additives
smoking
Psychosocial
Contributions
ADHD children are often viewed negatively by
others
Treatment of ADHD
Biological
Goal: reduce impulsivity and
hyperactivity, improve attention
Stimulant medications
Ritalin, Dexedrine, Adderall
risk for later
non-stimulant medications
Strattera and Qelbree
aren’t always as effective
Other medications - limited efficacy
Imipramine and clonidine (antihypertensive)
Effects of medications
decrease negative behaviors
Do not affect learning/academics directly
Benefits are not lasting
Behavioral approach treatment
Reinforcement programs
parent education programs
Social skills training
Cognitive behavioral therapy
for adults to increase attention and
organization
SPECIFIC LEARNING DISORDER
Types
impairment in reading
impairment in written expression
impairment in mathematics
Statistics
Prevalence of learning disorders
5 to 15%
Highest rate - wealthier regions but low SES more likely to have difficulties
Reading difficulties most common - 7%
Students with learning disorders
Drop out of school
unemployed
suicidal thought
negative school experiences
May be related to communication disorders
childhood-onset fluency disorder (stuttering)
langguage disorder
Causes
word recognition
genes
located on chromosomes 1, 2, 3, 6, 11, 12, 15, and 18
surroundings
brain impairment
three areas of the left hemisphere - dyslexia
left parietotemporal area
word analysis
left occipitotemporal area -
recognizing word form
left hemisphere—the
intraparietal sulcus - sense of numbers - mathematics disorder
Psychosocial contributions
Performance also influenced by
Motivational factors
Socioeconomic status
Cultural expectations
Parental interactions
Child management practices
Treatment
intense educational interventions
behavioral educational interventions
biological intervention
AUTISM SPECTRUM DISORDER
Two main areas of impairment
Communication and social interaction
10% to 33% don’t acquire effective speech
Restricted, repetitive patterns of behavior,
interests, or activities
Three levels of severity
Level 1— “Requiring support”
Level 2— “Requiring substantial support”
Level 3— “Requiring very substantial
support”
Two major characteristics of ASD are expressed in
DSM-5
Impairment in Social Communication and
Interaction
Failure to develop age-appropriate social
relationships
Trouble initiating and maintaining relationships
Trouble with nonverbal communication
lack appropriate expressions, tone
Trouble with social reciprocity
Deficits in joint attention
inability to communicate interest in
an external stimulus and another person at the same time
repeat the speech of others
echolalia
Restricted or Repetitive Behaviors and Interests
maintenance of
sameness
extremely upset if even a small change
was introduced
Severe forms -
Stereotyped or ritualistic behavior
spinning, waving hands, rocking
Less severe - interest in very specific
subjects
Prevalence
commonly diagnosed in males
4-5:1
IQ interaction
31% show intellectual disabilities
Occurs worldwide
Psychological and Social
Dimensions
Historical views
Failed parenting
lack of self-awareness
Biological Dimensions
genetic component
Numerous genes on several chromosomes
Older parents - increased risk
Oxytocin receptor genes- low level
Neurobiological influences
Amygdala
Larger size at birth
Elevated cortisol
Neuronal damage
Vaccinations do NOT increase the risk of autism
Treatment
Psychosocial
Behavioral approaches
Biological
Some drugs decrease agitation
Tranquilizers
SSRIs
Integrated
Preferred model: Multidimensional,
comprehensive focus
Intellectual Disability (Intellectual
Development Disorder)
IQ typically below 70-75
DSM-5 specifies deficits in
intellectual functioning and adaptive functioning during developmental period
Levels
Mild - IQ = 50 or 55 to 70
Moderate - IQ = 35-40 to 50-55
Severe - IQs = 20-25 to 35-40
Profound - IQ = below 20-25
DSM-5 identifies difficulties in three domains
Conceptual
Social
Practical
Statistics
Prevalence = 1-3% of general
population
9 in 10 people with ID have mild
impairment (IQ 50-70)
cronic course
Causes
Environmental
neglect, abuse
Prenatal
exposures to toxins in the womb
Perinatal
problems with delivery
Postnatal
infection and head injury
Genetic influences
Chromosomal
disorders
Down
Syndrome
xtra 21 cromosome
Multiple genetic
mutation
De novo disorders
Lesch-Nyham syndrome
Intellectual disability, symptoms of cerebral palsy self-injurious behavior, including finger and lip
biting
Only males are affected,- e X
chromosome in males does not have normal gene to balance.
Phenylketonuria (PKU)
cannot break down phenylalanine, which
is found in some foods
Fragile X syndrome- abnormality on the X chromosome
Symptoms
Gender differences
Primarily affects males- do not have second X cromosome
Women with Fragile X have mild symptoms
Learning disabilities
Hyperactivity
Short attention span
Treatment
Severe ID: Treatment similar to that for autism
spectrum disorder
Mild ID: Treatment similar to that for learning disorders
Behavioral interventions
Basic skills
dressing, hygiene
Social skills
Practical skills
paying bill
Augmentative strategies
use picture
books
make a request
by pointing to a picture
computer-assisted devices
presses a button to produce complete spoken sentences
Common goals
Participate in community life
Benefit from education
Build meaningful relationships
PREVENTION
Efforts in early stages
Early interventions
Head Start Program
Future directions
Genetic screening
OTHERS DISORDER
Language Disorder
Social ( Pragmatic) Communication
Tourette’s Disorder
Genetic and neurobiological contributions
Childhood Stuttering Fluency Disorder