Autism & Developmental

Autism Symptomatology in Boys with Fragile X Syndrome: A Cross Sectional Developmental Trajectories Comparison with Nonsyndromic Autism Spectrum Disorder.

Thurman et al. (2015) · Journal of autism and developmental disorders 2015
★ The Verdict

Autism traits in fragile X boys travel a different timeline, so measure progress against language or cognitive age, not calendar age.

✓ Read this if BCBAs who evaluate or treat boys with fragile X syndrome in clinic or school settings.
✗ Skip if Practitioners working only with nonsyndromic ASD and no genetic caseload.

01Research in Context

01

What this study did

Thurman et al. (2015) compared how autism traits unfold in boys with fragile X syndrome versus boys with classic autism. They mapped symptom timing against three yardsticks: age, nonverbal IQ, and number of words the child can say.

The team used a cross-sectional snapshot design. They placed each boy on a timeline to see when social, communication, and repetitive behaviors first appeared and how they changed.

02

What they found

Autism signs in fragile X boys did not follow the same path seen in nonsyndromic ASD. When the researchers lined up scores by vocabulary or IQ instead of birthday, the two groups landed at different points.

The data say the journeys diverge. Kids with fragile X reach similar autism totals, but they get there through a different route.

03

How this fits with other research

Falcomata et al. (2012) tracked the same fragile X group two years earlier. They showed that genetic syndrome, not starting IQ, best predicts later adaptive gains. John et al. extend that idea: the syndrome also shapes how autism features climb or level off.

van Rijn et al. (2014) ran a parallel comparison with children who have an extra X chromosome. Both studies use the same playbook—place a genetic syndrome beside idiopathic ASD and see where social skills land—giving clinicians two syndrome maps instead of one.

Burrows et al. (2018) pooled dozens of papers and found people with ASD make fewer facial expressions. Because fragile X boys often show social avoidance plus prominent eye-gaze aversion, the new trajectory data hint their expression drop-off may occur earlier or faster than in nonsyndromic peers.

04

Why it matters

If you assess a boy with fragile X, do not assume his autism graph will mirror classic ASD. Plot skills against language age or nonverbal ability, then set goals that match his actual curve. Update the plan as vocabulary grows; the slope may stay flatter for longer.

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Rescore the ADOS using the child’s language age instead of chronological age, then adjust the intervention sequence.

02At a glance

Intervention
not applicable
Design
other
Population
autism spectrum disorder, developmental delay
Finding
not reported

03Original abstract

Although males with fragile X syndrome (FXS) are frequently described as demonstrating autism symptomatology, there is much debate regarding whether the behavioral symptoms representing the core domains of autism are the result of the same or different underlying neurological/psychological mechanisms. The present study used a cross-sectional developmental trajectories approach to compare the profiles of autism symptomatology relative to chronological age (CA), nonverbal IQ, and expressive vocabulary ability between individuals with FXS and individuals with nonsyndromic ASD. Results suggest that the onset of autism symptoms and their developmental trajectories in males with FXS differ in important ways as a function of CA, nonverbal cognitive ability, and expressive vocabulary relative to males with nonsyndromic ASD. Theoretical and clinical implications are discussed.

Journal of autism and developmental disorders, 2015 · doi:10.1007/s10803-015-2443-4