School results in single-suture craniosynostosis: what should we tell parents at the first consultation? - 17/09/26
, Federica Moriconi b, Angelica Marfoli b, Giovani Dall’Olio b, Daniela Pia Rosaria Chieffo b, c, dHighlights |
• | Most children with nonsyndromic monosutural craniosynostosis achieve academic performance in the average range, but variability is increased and a meaningful subgroup benefits from educational supports. |
• | Real-world educational data show that meeting grade-level standards can coexist with evolving special education needs across primary school. |
• | Relative vulnerabilities are most consistently reported in mathematics, language-based learning processes, and attention/executive functioning-domains that shape classroom participation and homework load. |
• | Evidence does not support a robust independent effect of surgical timing or surgical approach on later school outcomes once confounding is considered; monitoring and early intervention remain appropriate regardless of technique. |
• | At first consultation, counselling should combine reassurance with a proactive plan: what to monitor, when to reassess, and how to collaborate with schools. |
Abstract |
Background |
Parents of children diagnosed with nonsyndromic single-suture craniosynostosis (SSC) frequently ask whether school difficulties should be expected and what type of monitoring is appropriate over time.
Objective |
To synthesize evidence on school-related outcomes in SSC and translate it into counselling guidance for the first consultation.
Methods |
We conducted a structured narrative review with a systematic literature search. PubMed/MEDLINE and Scopus were searched from database inception to January 2026 using terms related to craniosynostosis, single-suture disease, school achievement, learning, cognition, attention, executive function, behaviour, and educational supports. Reference lists of included studies and relevant reviews were hand-searched. Eligible sources included controlled cohorts, longitudinal studies, population or registry studies, systematic reviews/meta-analyses, and clinically relevant studies reporting academic, neuropsychological, behavioural, or educational service outcomes in children with nonsyndromic SSC. Results were narratively synthesized by school-relevant domains.
Results |
Mean intellectual and academic scores in SSC generally fall within normative ranges, with modest group differences and substantial overlap with peers. However, variability is increased, and a clinically meaningful subgroup shows learning vulnerabilities or requires educational supports. Mathematics, language-based learning processes, attention/executive function, and behaviour regulation are recurrent areas of concern. Population-linked and registry studies suggest that many children meet grade-level standards, while educational needs may emerge or become more visible as academic demands increase. Evidence for independent effects of surgical timing or technique on school-age cognition remains mixed and confounded.
Conclusions |
School outcomes in nonsyndromic SSC are generally favourable but heterogeneous. First-consultation counselling should combine realistic reassurance with anticipatory monitoring, attention to risk modifiers, and early collaboration with schools.
Le texte complet de cet article est disponible en PDF.Keywords : single-suture craniosynostosis, school outcomes, academic achievement, educational supports, executive function, CBCL, counselling, structured narrative review.
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