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Exam (elaborations)

Autism Spectrum Disorder (Peds) Questions and Answers

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Autism Spectrum Disorder (Peds) Incidence for Autism: - Answer- 1 in 59; 4x more common in boys than girls Cause of Autism: - Answer- There is a Genetic predisposition (but an unknown cause) Studies have shown that among identical twins, if one child has ASD, then the other will be BLANK a...

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  • August 26, 2024
  • 2
  • 2024/2025
  • Exam (elaborations)
  • Questions & answers
  • Autism Spectrum Disorder
  • Autism Spectrum Disorder
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Freshy
Autism Spectrum Disorder (Peds)
Incidence for Autism: - Answer- 1 in 59; 4x more common in boys than girls

Cause of Autism: - Answer- There is a Genetic predisposition (but an unknown
cause)

Studies have shown that among identical twins, if one child has ASD, then the other
will be BLANK about 36-95% of the time. In non-identical twins, if one child has ASD,
then the other is BLANK about 0-31% of the time - Answer- affected

ASD tends to occur more often in people who have certain genetic or chromosomal
conditions. About 10% of children with autism are also identified as having: -
Answer- Down syndrome, fragile X syndrome, tuberous sclerosis, or other genetic
and chromosomal disorders.

Almost half (44%) of children identified with ASD has: - Answer- average to above
average intellectual ability.

Children born to older parents are at a higher risk for having: - Answer- ASD

Difference between DSM4 and DSM5: - Answer- in DSM4 there was Pervasive
Developmental Disorders
(Autistic Disorder, Asperger's Disorder, Rett's Disorder, Childhood Disintegrative
Disorder, Pervasive Developmental Disorder) and in DSM5 these fall under Autism
Spectrum Disorders (levels 1-3).

Comorbidities of Autism: - Answer- -Diagnoses such as ID or LD
Genetic disorders
Biologically based behaviors such as tics
Medical conditions such as epilepsy

Common Genetic Disorders Associated with ASD: - Answer- Rett's syndrome (61%)
Tuberous Sclerosis complex (36%)
Fragile X syndrome (22-30%)
Neurofibromatosis (18%)
Down syndrome (16%)
William's syndrome (12%)
22q deletion syndrome (11%)

Persistent deficits in social communication and social interaction across contexts, not
accounted for by general developmental delays, and manifest 3 of 3 symptoms: -
Answer- -Deficits in social-emotional reciprocity
-Deficits in nonverbal communicative behaviors
-Deficits in developing, maintaining and understanding relationships

Restricted, repetitive patterns of behavior (RRB), interests, or activities as
manifested by at least 2 out of 4 symptoms: - Answer- Insistence on sameness

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