Abstract
Syndromic craniosynostoses are commonly treated conditions in craniofacial units. The features of the common syndromes (Apert, Pfeiffer and Crouzon) all include craniosynostosis, mid-face hypoplasia and ocular proptosis. The craniofacial management of a child with these syndromes through to adulthood may require a number of surgical interventions to allow brain development, to provide an adequate airway, to prevent corneal ulceration and to provide a functional dental occlusion. The management of these different priorities into timed interventions in our unit is determined by established protocols. We report two cases that underwent simultaneous mid-face (Le Fort III) and fronto-orbital osteotomies followed by distraction but using different vectors to advance the upper and mid-face regions (to achieve all treatment goals) in a 12-year-old boy and a 16-year-old girl.
Original language | English |
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Pages (from-to) | 626-631 |
Number of pages | 6 |
Journal | British Journal of Plastic Surgery |
Volume | 58 |
Issue number | 5 |
DOIs | |
Publication status | Published - Jul 2005 |
Externally published | Yes |
Keywords
- Apert syndrome
- Distraction osteogenesis
- Osteotomy
- Pfeiffer syndrome