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Evolutionary degeneracy theory
A 19th-century belief that intellectual and social challenges in children with IDD reflected regression to an earlier stage of human evolution; they were seen as the “missing link” between humans and lower forms.
Eugenics movement (1910)
Movement promoting societal protection from those with IDD; labeled mildly impaired individuals as “morons.”
Neurodevelopmental disorders
Lifelong disorders that have an onset at birth affecting the development of the brain and nervous system, leading to difficulties with learning, behaviour and social skills.
Genetic contribution to intelligence
Genetic factors account for 40–60% of variance in generalized intelligence.
Brain size correlation
Correlation between brain size and generalized intelligence is approximately .45.
Brain efficiency and intelligence
Individuals with higher intelligence show more efficient brain functioning.
Intelligence conceptualization
Defined in terms of an Intelligence Quotient (IQ).
Adaptive functioning
How effectively an individual copes with ordinary life demands and lives independently according to community standards.
General intellectual functioning
Measured by IQ tests that are standardized and individually administered.
IQ stability
IQ is relatively stable after early childhood; mean = 100, SD = 15.
Environmental influence on IQ
Mental ability can be modified by environment; SES explains variance in IQ.
Flynn effect
Average IQ scores rise ~3 points per decade; tests must be updated to reflect increasing intelligence.
IQ concerns
Lower mean IQ scores reported for Black individuals; debate over 80% heritability; environment remains crucial.
Multiple intelligences (Gardner)
Framework proposing several types of intelligence; rejects traditional IQ testing.
Diagnostic criteria for IDD
Deficits in intellectual and adaptive functioning evident during childhood or adolescence. Concurrent (regardless of environment) and evident during childhood or adolescence.
Degrees of IDD severity (DSM-5)
Mild, Moderate, Severe, Profound.
Degrees of IDD support (AAIDD)
Intermittent, Limited, Extensive, Pervasive.
Mild IDD
85% of cases; difficulties in academics, abstract thinking, executive functioning; immature social interactions; age-appropriate self-care but needs help with complex tasks.
Moderate IDD
10% of cases; slow academic skills; basic language; needs ongoing support for communication, personal care, and work; often benefits from group homes.
Severe IDD
4% of cases; minimal understanding of written language/time/money; limited speech; needs help with hygiene and self-care; requires full-time support.
Profound IDD
2% of cases; aware only of physical world; minimal communication; dependent on others for all tasks; often co-occurring motor/sensory impairments.
Prenatal risk factors (biomedical)
Genetic/chromosomal disorders, metabolic issues, maternal illness, parental age.
Prenatal risk factors (social/behavioral)
Poverty, malnutrition, domestic violence, substance use, lack of care or parental maturity.
Perinatal risk factors
Biomedical: Prematurity, birth injury, neonatal disorders, Social: parental rejection, Educational: missed medical follow-up.
Postnatal risk factors
Biomedical: TBI, malnutrition, infections, Social: poverty, neglect, abuse, poor stimulation,Educational:M delayed diagnosis, poor education/support.
IDD causes
2/3 of moderate to profoudn have genetic or environmental cause, causes for mild only ¼ are known.
Organic cuases two group approach
Organic intellectual deficit and cultural-familial intellectual deficit
Organic intellectual deficit
IDD caused by chromosome abnormalities, single-gene conditions, or neurobiological factors. Associated with severe and profound.
1/3 to ½ of people with IDD
Cultural-familial intellectual deficit
No clear organic basis and associated with mild IDD; family history of intellectual deficit, economic deprivation, inadequate child care, poor nutrition and parental psychopathology.
Heritability of intelligence
Estimated at 50%; environment strongly influences outcomes, especially for disadvantaged children.
Genotype
Collection of genes influencing intelligence.
Phenotype
Expression of genotype shaped by environmental interactions.
Heritability (definition)
Proportion of trait variation in a population attributable to genetic factors.
Most common cause of moderate to severe IDD
Chromosome abnormalities
Down syndrome
Extra 21st chromosome; ~1 in 1,000 births; caused by nondisjunction (21st pair of mothers chromosome doesn’t separate during meiosis); risk increases with maternal age. Have moderate IDD, equivalent to 2-3 year odl.
Fragile X syndrome
Most common inherited IDD from FMR-1 gene; 1 in 4,000 males / 1 in 8,000 females; mild to moderate IDD shyness, poor eye contact, repetitive behaviors.
1/3 to 1/2 of females who carry and transmit disorder are also affected with a variant of the syndrome.
20% of males with FMR1 transmit but not affected themselves.
Prader-Willi syndrome
Abnormal chromosome 15; intellectual deficits, short stature, constant hunger, low muscle tone. 5-10 out of 10 000 births; rare.
Phenylketonuria (PKU)
Single gene condition, Recessive gene disorder; lack of enzyme converting phenylalanine to tyrosine; buildup causes brain damage and IDD (errors of metabolism) 1 in 15000. Can be treated by environmental changes.
Angelman syndrome
Chromosome 15 disorder; moderate to severe IDD, jerky movements, hand flapping, seizures, absent speech.
Neurobiological causes
Adverse biological conditions
Infancy and childhood experiences
Prenatal alcohol exposure
Fetal alcohol spectrum disorder (FASD)
Caused by prenatal alcohol exposure; includes CNS dysfunction and developmental deficits.
Fetal alcohol syndrome (FAS)
Most severe form of FASD; growth retardation, facial anomalies, IDD, ADHD-like symptoms; 6–9 per 1,000 school-aged children.
Leading known cause of IDD
Social-psychological factors
Deprivation of care and stimulation; parental abuse or neglect; accounts for 15–20% of IDD cases.
Prevalence of IDD
1–3% of population; 1.5–2× more common in males; higher in lower SES and minority groups. 1.6 M to 1 F
Why are there SES differences?
Less access to quality education, home environment, economic deprivation
Developmental vs Difference Controversy
Do all children—regardless of intellectual impairments—progress through the same developmental milestones ina similar sequence, but at different rates? Or do children with intellectual developmental disorder develop in a different, less sequential, and less organized fashion?
Developmental position better aligns with…
familial intellectual developmental disorder as they follow developmental stages in an invariant order, the same as children with typical intellectual abilities, with the possible exception of some children with co-occurring brain differences or autism
Difference positon better aligns with
organic developmental disorder
2 approaches of the developmental position
Similar sequence and similar structure
Similar sequence hypothesis
Children with IDD follow same developmental stages as peers but at slower rates or lower limits.
Similar structure hypothesis
Children with IDD use the same cognitive processes as typically developing peers at similar cognitive levels.
Difference position
Cognitive development differs qualitatively, not just quantitatively, from typically developing peers.
Language and social development in IDD
Weak expressive language (especially in Down syndrome); delayed self-recognition; fewer signals for attachment.
Emotional/behavioral problems in IDD
4× higher than general population; includes impulse control, anxiety, mood, ADHD symptoms, pica, and self-injury.
Anxiety and IDD
Higher anxiety rates; elevated separation anxiety at age 5; often co-occurs with externalizing behaviors.
Health in IDD
Higher chronic illness rates; life expectancy in Down syndrome ≈ 60 years; cognitive decline common after 40.
Prevention and education
Prenatal education, genetic screening, ultrasounds, and awareness about substances during pregnancy.
Psychosocial treatments
Child-focused early intervention (ideally preschool years); behavioural techniques, cognitive behavioural and family oriented strategies.
Carolina Abecedarian Project
Early intervention for low-income children; led to reduced IDD rates and higher academic achievement.
Behaviour therapy and CBT for IDD
Target antecedents, consequences, or skill acquisition; interventions tailored to individual and environmental needs.
Communication interventions
Use of simplified, structured adult language to enhance understanding.
Routines and choices
Structured schedules with opportunities for personal choice increase engagement and independence.