Posterior vault distraction osteogenesis in Apert syndrome

Apert syndrome is an uncommon autosomal dominant condition with a varied clinical spectrum which includes  premature cranial and facial suture fusion and complex upper and lower limb syndactilies. In this manuscript, we share our posterior vault distraction osteogenesis (PVDO) experience regarding A...

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Main Authors: Cassio Raposo-Amaral (Author), Cesar Augusto Raposo-Amaral (Author), Enrico Ghizoni (Author)
Format: Book
Published: Brazilian Society for Pediatric Neurosurgery, 2022-05-01T00:00:00Z.
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100 1 0 |a Cassio Raposo-Amaral  |e author 
700 1 0 |a Cesar Augusto Raposo-Amaral  |e author 
700 1 0 |a Enrico Ghizoni  |e author 
245 0 0 |a Posterior vault distraction osteogenesis in Apert syndrome 
260 |b Brazilian Society for Pediatric Neurosurgery,   |c 2022-05-01T00:00:00Z. 
500 |a 2675-3626 
500 |a 10.46900/apn.v4i2(May-August).130 
520 |a Apert syndrome is an uncommon autosomal dominant condition with a varied clinical spectrum which includes  premature cranial and facial suture fusion and complex upper and lower limb syndactilies. In this manuscript, we share our posterior vault distraction osteogenesis (PVDO) experience regarding Apert syndrome patients so that a larger patient population may benefit. In addition, we aimed to determine an onset of elevated intracranial pressure in the long term follow up. A retrospective study was performed on consecutive patients with syndromic craniosynostosis who were diagnosed with Apert syndrome, underwent PVDO between 2012 and 2019, and received at least 2 years of follow-up care. Demographic data, diagnosis, surgery related data, and outcome data (perioperative and mid-term complications and need for additional surgery), were verified by means of medical records, clinical photographs, radiographic images, and interviews with all included patients and/or their parents. The present study included 14 patients who were diagnosed respectively with Apert syndrome (n = 14). The average posterior advancement distance achieved was 19.37 ± 3.0 mm. Two patients included in this study presented major complications, but neither experienced permanent sequelae or a lethal course. Two Apert patients presented cerebral spinal fluid (CSF) leakage (Clavien-Dindo type II).   One patient presented a onset of elevated intracranial pressure at 4 years of follow up. PVDO is an effective procedure at alleviating intracranial pressure and present a low complication rate. 
546 |a EN 
690 |a apert syndrome 
690 |a craniosynostosis 
690 |a syndromic craniosynostosis 
690 |a syndrome 
690 |a apert 
690 |a craniofacial dysostosis 
690 |a craniofaciostenosis 
690 |a cranioestenosis 
690 |a Pediatrics 
690 |a RJ1-570 
690 |a Surgery 
690 |a RD1-811 
655 7 |a article  |2 local 
786 0 |n Archives of Pediatric Neurosurgery, Vol 4, Iss 2(May-August), Pp e1302022-e1302022 (2022) 
787 0 |n https://www.archpedneurosurg.com.br/sbnped2019/article/view/130 
787 0 |n https://doaj.org/toc/2675-3626 
856 4 1 |u https://doaj.org/article/0b764a4ef05e4e9db4d3c3dcde1c8170  |z Connect to this object online.