exam 4 intellectual disability (2)

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32 Terms

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Intellectual Disability

1.Intellectual functioning (intelligence) and

2.Adaptive behavior and

3.Onset must be before age 18

•Not an appropriate diagnosis for an adult with similar limitations due to a TBI experienced at age 21

•Generally nonprogressive

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Intellectual Disability – Characteristics of the Diagnosis

IQs that are 2SDs below the mean

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Intelligence is______ by standard tests with a strong presumption of this disability

unable to be tested

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global developmental delay (GDD)

Children who are younger than 5 years

  • Delayed achievement of developmental milestones

Temporary diagnosis

  • Reassessment needed after age 5

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Signs of delay (2 - 4 months)

Failure to interact with the environment

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Signs of delay (6 - 18 months)

Decreased gross motor skills

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Signs of delay (18 months - 5 years)

Decreased language development

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Signs of delay (3-5 years)

•Decreased or abnormal play and social skills

•Below age level fine motor skills

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Signs of delay (5+ years)

•Decreased academic achievement

Abnormal attention, anxiety levels, mood and conduct

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mild

can live indepedently with minimum levels of support 

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moderate

independet living may be achieved with moderate levels of support

  • lives in group homes

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severe 

requires daily assistance with self-care activities and safety supervison 

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profound

requires 24-hour care

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AAIDD the level of supports (intermittent)

as needed

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AAIDD the level of supports (limited)

a limited period of time

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AAIDD the level of supports (extensive)

daily in a life area

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AAIDD the level of supports (pervasive)

daily, all life areas, all contexts

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black children are ___ more likley to be diagnosies with intellectual disabilites

2x

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___ are more likely to be diagnosed with intellectual disabilities 

boys 

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Mild Intellectual Disabilities cause 

Environmental factors such as socioeconomic status and neglectful or abusive caregivers.

•Diagnosis may be late

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Severe Intellectual Disabilities causes

Biomedical origin (genetic, non-genetic congenital birth anomalies)

Greater number of associated impairments

  • ex: Cerebral palsy, seizures, sensory issues

Diagnosis as a newborn or infant due

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Single gene disorders (Biomedical Influences)

•Autosomal dominant: Tuberous sclerosis

•Autosomal recessive: Tay-Sachs, phenylketonuria

•X-linked: Fragile X syndrome

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Chromosomal disorders (Biomedical Influences)

•Down syndrome (trisomy 21)

•Trisomy 18, 13

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Prenatal (Environmental Influence)

  • Prematurity

  • mom gets infection

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Perinatally (Environmental Influence)

  • While giving birth

birth injuries during difficult labors

Acquire HIV-1- giving it to the baby

Hypoxia (decreased oxygen supply)

premature birth

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Postnatally (Environmental Influence)

•Trauma with injury or lack of oxygen to the brain

  • Infections with injury

  • Severe psychosocial deprivation

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Early Signs and Symptoms

young child

  • limitations in recalling information

  • understanding consequences

  • social rules

  • difficulty problem solving

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Mild ID

•A child may have difficulty learning an academic skill, challenges with abstraction, EF, STM

•Adults may have a concrete approach to problem solving

•Immature social interactions

•May be IND in ADLs and may be employable

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Moderate ID

•A child may have slow development of language/academic skills in pre-K

•Adults may have an elementary-level education

•May require repetition of teaching and reminders to support ADLs and recreational skills

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Severe ID

•Expressive language – single words, phrases, AAC means

•Receptive language – simple speech, gestures

•High level of support needed for problem solving

•Require Supervision

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Profound ID

•Expressive and receptive language very limited, gestures and emotional cues may be used and understood

•Recreation may include water activities, walking, listening to music, watching movies

•Dependent in ADLs or may be able to assist caregiver

•May be able to functionally use objects

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Life expectancy is similar to general population for those with _____

mild ID