Literature DB >> 28820838

Five-Year Follow-Up of Midface Distraction in Growing Children with Syndromic Craniosynostosis.

Parit A Patel1, Pradip R Shetye, Stephen M Warren, Barry H Grayson, Joseph G McCarthy.   

Abstract

BACKGROUND: Maxillary position in patients with syndromic craniosynostosis after midface distraction has been shown to be stable 1 year postoperatively. The purpose of this study is to assess midfacial position in the growing child with craniosynostosis 5 years after Le Fort III advancement with a rigid external device.
METHODS: Seventeen consecutive patients were identified to have the diagnosis of syndromic craniosynostosis and had undergone midface advancement [corrected]. There were 10 boys and seven girls, seven patients had Crouzon syndrome, five had Apert syndrome, and five had Pfeiffer syndrome. A standard subcranial Le Fort III osteotomy was performed. Cephalometric analysis was performed to assess the position of the maxilla.
RESULTS: After device removal, orbitale advanced 13.67 mm along the x axis and downward 1.70 mm along the y axis. The A point advanced 15.97 mm along the x axis and downward 1.14 mm along the y axis. At 1 year after distraction, both orbitale and A point had advanced an additional 0.47 mm and 0.24 mm along the x axis and downward 0.58 mm and 1.78 mm along the y axis, respectively. At 5 years after distraction, the orbitale moved posterior 0.58 mm and the A point advanced an additional 2.08 mm along the x axis. Orbitale and A point descended 3.23 mm and 5.2 mm along the y axis, respectively.
CONCLUSION: After Le Fort III advancement with distraction, the maxillary position remains stable and continues to advance minimally along the x axis and demonstrates more growth along the y axis over the long term. CLINICAL QUESTION/LEVEL OF EVIDENCE: Therapeutic, IV.

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Year:  2017        PMID: 28820838     DOI: 10.1097/PRS.0000000000003879

Source DB:  PubMed          Journal:  Plast Reconstr Surg        ISSN: 0032-1052            Impact factor:   4.730


  2 in total

1.  Severe craniolacunae and upper and lower extremity anomalies resulting from Crouzon syndrome, FGFR2 mutation, and Ser347Cys variant.

Authors:  Cassio Eduardo Raposo-Amaral; Yuri Moresco Oliveira; Rafael Denadai; Cesar Augusto Raposo-Amaral; Enrico Ghizoni
Journal:  Childs Nerv Syst       Date:  2021-01-06       Impact factor: 1.475

Review 2.  Non-invasive Ventilation and CPAP Failure in Children and Indications for Invasive Ventilation.

Authors:  Alessandro Amaddeo; Sonia Khirani; Lucie Griffon; Theo Teng; Agathe Lanzeray; Brigitte Fauroux
Journal:  Front Pediatr       Date:  2020-10-26       Impact factor: 3.418

  2 in total

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