# Cognitive and neuropsychomotor development in craniosynostosis: an evaluation of the most affected functions

**Authors:** Jéssica Luchi Ferreira, Igor José Nogueira Gualberto, Mariani Da Costa Ribas, Michele Madeira Brandão, Cristiano Tonello

PMC · DOI: 10.1007/s00381-026-07127-w · 2026-01-29

## TL;DR

This study examines how craniosynostosis affects cognitive and motor development, finding significant differences between syndromic and isolated cases.

## Contribution

The study provides a detailed characterization of cognitive and neuropsychomotor profiles in craniosynostosis patients.

## Key findings

- 68.4% of syndromic patients showed altered neuropsychological results.
- Language skills were most frequently affected, with fluid intelligence deficits in 45.5% of patients.
- Early surgery correlated with better cognitive outcomes, while later surgery was linked to poorer results.

## Abstract

The physical manifestations of craniosynostosis are well-documented, but its impact on neurodevelopment and cognitive functions remains under-researched. Evaluating neurodevelopment and cognition is essential to establish baseline cognitive functions in surgical procedures, guiding therapeutic and rehabilitation strategies post-surgery. This study aims to characterize the cognitive profile and neuropsychomotor development in individuals with craniosynostosis, identifying the most affected functions.

This study was a retrospective, observational, cross-sectional chart review that analyzed 65 individuals with craniosynostosis (39 syndromic, 26 isolated) who underwent neuropsychological assessments. Five key instruments were used to assess neuropsychomotor development and cognitive functions across different age groups.

Significant neuropsychological differences were found between syndromic and isolated groups (p = 0.026). Key findings include the following: 68.4% of syndromic patients showed altered neuropsychological results; 40.7% of the isolated group demonstrated neuropsychological variations; language skills most frequently affected; fluid intelligence deficits in 45.5% of patients; motor gross impairments in 24.0%, predominantly in the isolated group. A weak negative correlation was observed between surgery age and cognitive improvement (r = −0.32), with early surgery (0–1 year), mixed outcomes, and later surgery (3 + years), poorer cognitive results.

Early interventions are crucial for reducing developmental delays, though individual variability and syndromic conditions significantly influence outcomes. Focusing on early intervention, targeted rehabilitation, and smooth school transition can optimize cognitive development and manage potential delays.

The online version contains supplementary material available at 10.1007/s00381-026-07127-w.

## Linked entities

- **Diseases:** craniosynostosis (MONDO:0015469)

## Full-text entities

- **Genes:** TWIST1 (twist family bHLH transcription factor 1) [NCBI Gene 7291] {aka ACS3, BPES2, BPES3, CRS, CRS1, CSO}, FGFR1 (fibroblast growth factor receptor 1) [NCBI Gene 2260] {aka BFGFR, CD331, CEK, ECCL, FGFBR, FGFR-1}, FGFR2 (fibroblast growth factor receptor 2) [NCBI Gene 2263] {aka BBDS, BEK, BFR-1, CD332, CEK3, CFD1}, FGFR3 (fibroblast growth factor receptor 3) [NCBI Gene 2261] {aka ACH, CD333, CEK2, HSFGFR3EX, JTK4}
- **Diseases:** Motor impairments (MESH:D000068079), developmental delays (MESH:D002658), CFND (MESH:C536456), cranial deformity (MESH:D003389), language alterations (MESH:D007806), absence (MESH:D004832), gross and fine motor impairments (MESH:D014202), gross (MESH:C536704), Crouzon (MESH:D003394), motor and communication impairments (MESH:D003147), NPA (MESH:D008607), PIQ deficits (MESH:D009461), Adaptive-behaviour impairments (MESH:D018489), COVID-19 (MESH:D000086382), Craniosynostosis (MESH:D003398), FSIQ impairments (MESH:C538175), Language and motor delays (MESH:D007805), impairments in gross motor skills and adaptive behaviour (MESH:D019957), -Chotzen (MESH:D000168), cognitive alterations (MESH:D003072)
- **Chemicals:** FFMA (MESH:C100324)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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Source: https://tomesphere.com/paper/PMC12852296