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Published on: November 4, 2025
Craniofacial disorders associated with airway obstruction in the neonate
Christopher M Cielo1, Fernando M Montalva2, Jesse A Taylor3
1Perelman School of Medicine at the University of Pennsylvania, Division of Pulmonary Medicine, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Insights
Infants with craniofacial disorders often experience upper airway obstruction, a serious risk for neonatal mortality. This review focuses on evaluating and managing this condition, particularly in Pierre Robin sequence.
Area of Science:
- Neonatal Medicine
- Pediatric Surgery
- Genetics
Background:
- Upper airway obstruction (UAO) is a major cause of morbidity and mortality in neonates with craniofacial disorders.
- Infants with conditions like Pierre Robin sequence have a high risk of obstructive sleep apnea syndrome.
- Multidisciplinary team care is essential for timely evaluation and optimal management of these complex cases.
Purpose of the Study:
- To review the current literature on the evaluation and management of UAO in neonates with craniofacial conditions.
- To specifically address the challenges and approaches for Pierre Robin sequence.
- To highlight recent advances and remaining questions in the field.
Main Methods:
- Literature review of studies on neonatal UAO and craniofacial disorders.
- Focus on diagnostic tools including history, physical examination, genetic testing, imaging, endoscopy, and polysomnography.
- Analysis of various surgical and non-surgical treatment options.
Main Results:
- Craniofacial disorders significantly increase the risk of UAO and obstructive sleep apnea in neonates.
- A comprehensive evaluation involving multiple diagnostic modalities is crucial.
- Treatment strategies are diverse, ranging from conservative to surgical interventions, tailored to individual patient needs.
Conclusions:
- Effective management of UAO in neonates with craniofacial disorders requires a multidisciplinary approach.
- Early and accurate diagnosis is key to preventing severe outcomes.
- Continued research is needed to further refine assessment and treatment protocols, especially for Pierre Robin sequence.
Abstract:
In infants with craniofacial disorders, upper airway obstruction is one of the primary causes for morbidity and mortality in the neonatal period. Infants with craniofacial disorders, including Pierre Robin sequence, are at high risk for obstructive sleep apnea syndrome. Because of the complexity of their care, these neonates are usually followed by a multidisciplinary team to ensure timely evaluation and optimal treatment. In addition to history and physical examination, clinical evaluation may include genetic testing, imaging, endoscopy, and polysomnography. There are various treatment options, both surgical and non-surgical, that may be used depending on clinical assessment, underlying condition, and severity of disease. Recent advances have led to better assessment and treatment of these patients, but many questions remain. This review outlines the available literature pertaining to the evaluation and management of upper airway obstruction in the neonate with craniofacial conditions, with a particular focus on Pierre Robin sequence.
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