Literature DB >> 25650655

Monobloc Le Fort III Distraction Osteogenesis for Correction of Severe Fronto-orbital and Midface Hypoplasia in Pediatric Crouzon Syndrome.

Firdaus Hariri, Lim Kwong Cheung, Zainal Ariff Abdul Rahman, Vickneswaran Mathaneswaran, Dharmendra Ganesan.   

Abstract

In severe syndromic craniosynostosis, distraction osteogenesis (DO) provides superior segmental advancement and allows progressive clinical monitoring to ensure that adequate skeletal expansion is achieved. We report two cases of Crouzon syndrome involving a 3-year-old boy and a 4-year-old girl, who were both treated with monobloc Le Fort III DO using a combination of external and internal distraction devices (Synthes, Oberdorf, Switzerland) to treat severe orbital proptosis and obstructed nasopharyngeal airway secondary to severe hypoplastic craniofacial skeletal components. Their skeletal segments were advanced in daily increments by 27 mm and 23 mm, respectively. Results at 18 months postoperatively showed successful outcomes, as evidenced by adequate eye protection, tracheostomy tube decannulation following objective evidence of patent nasopharyngeal airway, and acceptable facial appearance. Monobloc Le Fort III DO using a combination of external and internal devices produces favorable functional and clinical outcomes for the treatment of severe orbital and airway discrepancy in Crouzon syndrome.

Entities:  

Keywords:  Crouzon syndrome; craniofacial surgery; distraction osteogenesis; monobloc Le Fort III

Mesh:

Year:  2015        PMID: 25650655     DOI: 10.1597/14-210

Source DB:  PubMed          Journal:  Cleft Palate Craniofac J        ISSN: 1055-6656


  4 in total

1.  The utilisation of 3D printing in paediatric neurosurgery.

Authors:  Ravindran Karuppiah; Thangaraj Munusamy; Nor Faizal Ahmad Bahuri; Vicknes Waran
Journal:  Childs Nerv Syst       Date:  2021-03-18       Impact factor: 1.475

Review 2.  Crouzon syndrome: Genetic and intervention review.

Authors:  N M Al-Namnam; F Hariri; M K Thong; Z A Rahman
Journal:  J Oral Biol Craniofac Res       Date:  2018-08-29

3.  Inherited FGFR2 mutation in a Chinese patient with Crouzon syndrome and luxation of bulbus oculi provoked by trauma: a case report.

Authors:  Ji Yang; Tao Tao; Hai Liu; Zhu-Lin Hu
Journal:  BMC Ophthalmol       Date:  2019-10-22       Impact factor: 2.209

4.  An Unoperated Crouzon Family Treated with Monobloc Distraction: Challenges and Lessons.

Authors:  Justin Hart; Stephen Lu; Konstantinos Gasteratos; Kongkrit Chaiyasate
Journal:  Plast Reconstr Surg Glob Open       Date:  2021-11-02
  4 in total

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