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Understanding normocephalic craniosynostosis: a case-control study on prevalence, clinical features, and
Sarut Chaisrisawadisuk1,2, Sirin Nittayakasetwat3, Sirin Apichonbancha3
1Division of Plastic Surgery, Department of Surgery, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand. sarut.cha@mahidol.ac.th.
Normocephalic craniosynostosis (NC) may have pathological implications despite no visible deformities. This study highlights increased male predominance and neurological issues in NC patients, suggesting a need for vigilant monitoring.
Area of Science:
- Pediatric Neurosurgery
- Developmental Neuroscience
- Medical Imaging
Background:
- Normocephalic craniosynostosis (NC) involves premature cranial suture fusion without external deformities.
- NC may be linked to neurodevelopmental risks, necessitating further investigation.
Purpose of the Study:
- To investigate the characteristics and potential associations of normocephalic craniosynostosis (NC).
- To identify demographic, clinical, and radiological factors related to NC.
Main Methods:
- A case-control study involving 42 NC patients and 41 controls aged 1-20 years.
- Data collected from CT scans and electronic medical records, including demographics, neurological symptoms, and comorbidities.
Main Results:
- No significant difference in cephalic index or age at scanning between NC cases and controls.
- A marked male predominance (83.3%) and higher incidence of abnormal neurological issues (35.7%) were observed in NC cases.
- A family history of abnormal neurodevelopment was noted in 4.8% of NC cases, though not statistically significant.
Conclusions:
- Findings suggest potential pathological implications of NC, warranting enhanced clinical vigilance.
- A multidisciplinary approach is crucial for optimal evaluation and management of NC patients.
- Further research is needed to fully understand NC despite the absence of external cranial deformities.
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