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[Synostosic and non-synostosic cranial deformities]
Gabriel A González1, Daniel Cruz2
1Servicio de Neuropediatría, Centro Hospitalario Pereira Rossell, Facultad de Medicina, Universidad de la República, Montevideo, Uruguay. E-mail: viciogon hotmail.com.
Insights
Positional plagiocephaly and craniosynostosis require different management. Early diagnosis is crucial for infants with skull shape alterations to ensure appropriate treatment and prevent developmental issues.
Area of Science:
- Pediatrics
- Neurosurgery
- Developmental Biology
Background:
- Increased incidence of infant skull deformities, particularly positional plagiocephaly, linked to supine sleep recommendations.
- Clinical differentiation between positional plagiocephaly and craniosynostosis is essential due to distinct management pathways.
Purpose of the Study:
- To outline diagnostic approaches for infant skull deformities.
- To differentiate between positional plagiocephaly and craniosynostosis.
- To guide management strategies for both conditions.
Main Methods:
- Clinical evaluation as the primary diagnostic tool.
- Three-dimensional skull tomography (bone window) for high sensitivity and specificity.
- Radiography or ultrasound for ambiguous cases.
Main Results:
- Craniosynostosis necessitates prompt referral to a craniofacial team for surgical planning.
- Positional plagiocephaly, even when treated, may be associated with a higher risk of motor development delay.
- Mild to moderate positional plagiocephaly can be managed with repositioning and physical therapy; severe cases may require cranial orthotics.
Conclusions:
- Accurate diagnosis is critical for appropriate infant skull deformity management.
- Timely intervention for craniosynostosis prevents long-term neurocognitive and psychosocial complications.
- Positional plagiocephaly management should address potential motor development delays alongside cranial correction.
Abstract:
In the last decades alterations in the skull shape have increased at the expense of plagiocephaly, as consequence of the American Academy of Pediatrics recommendations to sleep the infant in the supine position. The clinician must differentiate between positional plagiocephaly and craniosynostosis, since if a cranial synostosis is proven, the therapeutic behavior will be potentially neurosurgical. Although three-dimensional skull tomography with bone window is the study of greater sensitivity and diagnostic specificity, the majority of cases can be confirmed by the clinic, reserving the radiography or ultrasound with a suture approach for doubtful cases. Craniosynostosis must be early referral to a craniofacial team to define the indication, opportunity and most appropriate surgical technique, in order to avoid future neurocognitive and psychosocial complications. Children with positional plagiocephaly regardless of the treatment of cranial deformity may have a higher risk of motor development delay. For correction, repositioning and physiotherapy are suggested in mild to moderate forms, reserving the use of cranial orthesis in severe forms.
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