Neurodevelopmental Disorders (5)
ADHD
characterised by either inattention and/or hyperactivty/impulsivity
- can either have combined presentation, predominantly inattentive, or predominantly hyperactive
Inattention
inability to sustain focus, to organise, easily distracted, losing things easily, etc
Hyperactivity
interrupting, blurting out, unable to play quietly, problems with fidgeting, difficulty waiting
ADHD Prevalence
1/20 children worldwide could be diagnosed with this
ADHD Etiology
ADHD Treatment
Autism Spectrum Disorder Clusters (3)
Dimensional Aspects for Autism Spectrum Disorder (3 levels)
Autism Spectrum Disorder Prevalence
1/50 children
5:1 males
38% show intellectual disabilities as well
females more likely to have < IQ
20% likelihood of having another child w autism after having the first
Autism Spectrum Disorder Etiology
Autism Spectrum Disorder Treatment
-multidimensional comprehensive focus
- special education
- focus on communication
- medication, mayb
- support for families
- integrating adults into society
- independence maximisation
- dimensional aspects
Asperger’s Syndrome
Specific Learning Disorder(s)
characterised by the performance in a particular area that is substantially below what would be expected at IQ, age, etc
- response to intervention is used for diagnosis
Response to Intervention
how a child reacts to specific interventions that have been proven to be effective; if they are not as successful as their peers, it is a sign that they may have a SLD
Specific Learning Disorder Categories (3)
Specific Learning Disorder Etiology
Intellectual Disability (Intellectual Development Disorder)
characterised by significant impairment in many different areas of life that interferes with independence
Intellectual Development Disorder Categories (3)
American Association on Intellectual and Developmental Disabilities Support Scale (4)
Intellectual Developmental Disorder Etiology
Lesch-Nyhan Syndrome
Phenylketonuria
phenylalanine causes ID and seizures because it deposits in the brain
Down Syndrome/Trisomy 21