I found this online:
Suppose a genetic test for the BAP became available, and the following situation occurred:
Two siblings test positive for the BAP at birth.
No difference between them was noted during their first year of life.
An evaluation of both siblings at 3 years old found only one of them had ASD
At 20 years old, the sibling with ASD no longer met the criteria for ASD
A second evaluation of both siblings when they were 20 years old found they had the same autistic traits that are part of the BAP with no difference between them
How would you classify the sibling who was diagnosed with ASD?
"The presence of autism-related traits has been well documented in undiagnosed family members of individuals with autism spectrum disorder (ASD). The most common finding is mild impairments in social and communication skills that are similar to those shown by individuals with autism, but exhibited to a lesser degree. Termed the broader autism phenotype (BAP), these traits suggest a genetic liability for autism-related traits in families." The Broader Autism Phenotype and Its Implications on the Etiology and Treatment of Autism Spectrum Disorders
Suppose a genetic test for the BAP became available, and the following situation occurred:
Two siblings test positive for the BAP at birth.
No difference between them was noted during their first year of life.
An evaluation of both siblings at 3 years old found only one of them had ASD
At 20 years old, the sibling with ASD no longer met the criteria for ASD
A second evaluation of both siblings when they were 20 years old found they had the same autistic traits that are part of the BAP with no difference between them
How would you classify the sibling who was diagnosed with ASD?
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