Atypical development Flashcards

(45 cards)

1
Q

what is atypical development?

A

Someone whose development/cognitive processes differ more than typical individual variation, Different developmental patterns and/or, Developmental delays

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2
Q

The medical model approach atypical development

A
  • Tends to measure individuals against what is typical/the norm
  • Tends to work with a deficit view, identifying problems with individuals.
  • It then uses this to build knowledge as well as develop and provide treatment and support
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3
Q

From knowing that cognitive abilities are associated with a genetic disorder what else can we know?

A
  • We can infer how genes are involved in those cognitive abilities
  • And also infer how these genes affect development.
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4
Q

What is neuroconstructivism ?

A

Study of how genes and the environment interact over time and how it shapes the development of cognitive abilities.

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5
Q

What are key ideas emphasized by Neuroconstructivism?

A

Gene expression changes over time, just like cognitive abilities.

It’s difficult to tell if a cognitive trait is caused by a missing gene or by environmental influences that alter gene expression.

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6
Q

Single dissociation studies

A

One disorder is associated with a particular trait, E.g. language difficulties. If disorder is genetically well described this can tell us a lot. But are the genes associated with that disorder, atypical development in general or specifically language difficulties?

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7
Q

Double dissociation studies

A

TWo disorders - one is caused by one thing and the second by another thing

better for establishing if genes are associated with a disorder.

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8
Q

What is atypical intellectual syndrome?

A

Can often co-occur with conditions such as depression, ADHD, Autistic Spectrum Condition.

Consider those who perform significantly below average in - intellectual functioning or adaptive functioning.

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9
Q

when is the onset of atypical intellectual syndrome?

A

Onset of the condition is prior to the end of the developmental period - To mark it out as a developmental condition rather than occurring due to an event that happens later in life.

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10
Q

What are three domains of adaptive functioning?

A
  1. Conceptual ~ language skills, reading, writing
  2. Social ~ empathy, social judgement or interpersonal communication skills
  3. Practical ~ personal care or job responsibilities
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11
Q

What are the physical traits of William Sybdrone?

A
  • Cardiac, musculoskeletal, renal and dental differences
  • Hypercalcemia: extra calcium in their blood (associated with weaker blood and heart problems
  • Distinctive facial features
  • Small stature
  • Problems with binocular vision
  • Hyperacusis (heightened sensitivity to sound)
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12
Q

personality of williams syndrome

A
  • very friendly and gregarious.
  • Unafraid of strangers.
  • Empathetic, extremely trusting and accommodating.
  • More active than typical, difficulty with concentration (often co-occurs with ADHD).
  • Anxiety and phobias.
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13
Q

what are the cognitive strengths of someone with Williams syndrome?

A

Strengths: Language, Face recognition, Social Interaction skills

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14
Q

what are the cognitive weaknesses of someone with Williams syndrome?

A

Difficulties: Spatial & numerical skills , IQ falls into the lower range (40-90)

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15
Q

what is the genetic malfunction in people with Williams syndrome?

A

Not a certain gene - more pattern of gene deletion, in genes that are associated with physical traits.

Different groups within WS (7) each are associated with a different pattern of gene deletion.

This shows that even within those with WS, different patterns of gene deletion can be associated with different traits.

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16
Q

How do children with WS and DS perform differently when they have to describe a frog story?

A

WS - very expressive language at both 13 and 17

DS - not a lot of language - limited vocabulary

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17
Q

How is grammar and vocab different in WS and SW?

A

Grammar —> WS show good comprehension. Better grammar. Compared to DS.

Vocab —> Had to list animals and WS named more animals and uncommon ones compared to DS children.

Linguistic effect —> evidence those with WS use language that is affectively rich. WS outperform others.

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18
Q

How do WS compare to typically developing children?

A

WS compared to typical developing children. The proportion of incomplete sentences they use. (WS more than TYpical less than DS)

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19
Q

what disorder provides a double dissociation with WS?

A

Down Syndrome

20
Q

How does cognitive genetics relate to language processing?

A

Genes coding for language skills are present in individuals with Williams Syndrome (WS).

Double dissociations with disorders like Down syndrome, DLD, and dyslexia suggest different genetic impacts on language.

Helps identify genes linked to language abilities.

21
Q

How does neuroconstructivism explain language processing?

A

Missing genes may be linked to language impairment, but the reason why is unclear.

Gene-environment interactions in language development are still not well understood.

The same gene may affect language differently at various developmental stages.

22
Q

What does research say about social cognition in individuals with Williams Syndrome?

A

People with WS often use richer, more socially engaging language.

Adolescents with WS:

Use more socially evaluative language

Reference affective states more

Evaluate others’ behavior

Use emphatic markers (e.g., “really”, “for sure”, “certainly”)

23
Q

How do social interactions for WS and DS compare?

A

WS –> more likely to initiate dyadic interactions, with parents and even more with novel adults.

DS –> less likely to talk to someone they do not know

24
Q

How do adults with WS perform at face configuration tasks?

A
  • They could only say if faces were the same and be correct 51% compared to typical adults who got 75%
25
When face features were changed how did adults with WS perform?
the same as typical adults suggesting this is not a problem
26
what is the difference between facial features and configuration?
Facial features = the parts Face configuration = how the parts are arranged
27
How do people with WS respond to jokes?
- WS can struggle with distinguishing ironic jokes from lies. - Which may explain why clinical reports describe those with WS as often making poor social judgements.
28
What social challenges are often observed in individuals with Williams Syndrome?
They can often find it difficult to maintain friendships, despite showing strong social interest.
29
What does Williams Syndrome suggest about the genetics of social motivation?
It suggests that genes coding for systems that motivate typical social interest and interaction are present in individuals with Williams Syndrome.
30
How can double dissociations help identify genes related to social interest and cognition?
Comparing conditions like Williams Syndrome and Autism Spectrum Condition—where social interests differ—can help identify which genes are linked to typical social interest and cognition.
31
What does early development of social interest in Williams Syndrome suggest?
A strong interest in interacting with strangers develops early, suggesting a lower influence of the environment and a possible stronger genetic basis.
32
What do stable differences in facial recognition processing suggest?
That these differences are consistent from adolescence to adulthood, indicating less impact of environmental factors and more stable, possibly biological, origins.
33
in spatial tasks what do WS struggle with?
- WS draw the individual elements well but struggle to put the elements together in the right configuration. - Contracting a pattern, can pick up on detail but again struggle with the overall configuration of the pattern.
34
when creating a bigger shaper with smaller shapes how do WS perform?
Creating a bigger shape using smaller shapes – they can produce the smaller shapes but struggle with the bigger shape
35
how do DS and WS different in global and local details?
Down Syndrome —> Struggle with local detail, —> internal structure Williams Syndrome —>Struggle with global —> organization/configuration
36
Local processing bias theory
- Suggests a processing difference rather than deficit. - It’s not that those with WS can’t process global configurations, rather they just orientate more towards local details.
37
What were the two visual tasks given to children aged 4–15 in the study?
Task 1: Identify if concentric circles (form) were present on the left or right side of a display of small line segments. Task 2: Identify which of two displays showed dots moving in the opposite direction in the center (motion).
38
What did the results show in 4–5-year-old typically developing (TD) children ability at a motion task?
They were worse at motion than form, indicating a dorsal stream deficit at that age.
39
How did performance in TD children change by age 15 at the motion task?
Performance on motion and form tasks became equal, suggesting the dorsal stream deficit disappears with development.
40
How did children with Williams Syndrome (WS) perform on the tasks?
A small subset were consistently worse at motion than form up to age 15 → persistent dorsal stream deficit. Others were impaired on both motion and form → general global processing difficulties.
41
What do the findings suggest about dorsal and ventral stream processing in WS?
WS children show dorsal stream (motion) deficits. Many also show ventral stream (form) deficits. Suggests variation in global visual processing among individuals with WS.
42
What did adult brain imaging show in individuals with WS?
Adults with WS showed reduced activation in parietal lobe areas (part of the dorsal stream), supporting the hypothesis of dorsal stream impairment.
43
Does developmental data fully support the dorsal stream deficit hypothesis in WS?
Not entirely—while there is some support, the data shows variation among individuals, and the deficit is not universal.
44
What does cognitive genetics suggest about spatial cognition in Williams Syndrome?
Genes deleted in WS may be linked to dorsal stream development. Double dissociations (e.g., with Down Syndrome) can help identify which genes are linked to visuo-spatial processing.
45
What questions does neuroconstructivism raise about dorsal stream deficits in WS?
Are dorsal stream deficits a cause or an effect? Do structural abnormalities cause spatial issues, or does reduced spatial input from the environment lead to atypical dorsal stream development?