About site: Support Groups/Conditions and Diseases/Facial Differences/Craniosynostosis - The Craniofacial Group - Paris, France
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  About site: http://www.cranio-facial.org

Title: Support Groups/Conditions and Diseases/Facial Differences/Craniosynostosis - The Craniofacial Group - Paris, France Craniofacial Group; Management of anomalies of skull and face : craniosynostosis, facial clefts, hypertelorism, tumors and trauma.
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Craniofacial Group Paris-France: Management of anomalies of skull: craniostenosis,hypertelorism,Crouzon,Apert <b>Cranio<b>facial</b></b> Group: <b>Management</b> of <b>anomalies</b> of <b>skull</b> and face: craniostenosis, <b>craniosynostosis,</b> <b>facial</b> <b>clefts,</b> <b>hypertelorism,</b> Crouzon,Apert, <b>tumors</b> and trauma <b>Cranio<b>facial</b></b> Group - Paris, France Management of anomalies of skull and face: craniostenosis, craniosynostosis, facial clefts, hypertelorism, Crouzon, Apert, tumors and trauma - Daniel Marchac, MD, Plastic Surgeon - Dominique Renier, MD, Pediatric Neurosurgeon - Eric Arnaud, MD, Plastic Surgeon   and a pluridisciplinary team French version French version HomeHistoryConditions treatedPositionnal DeformitiesPrinciple of treatementTiming of treatementBibliographyContact For 25 years, our group, comprising the specialities of craniofacial and plastic surgery, and paediatric neurosurgery, has been dealing with craniofacial anomalies. Craniofacial surgery is especially involved with treating congenital craniofacial anomalies. The first group is represented by craniosynostosis or craniostenosis, in which the cranial sutures are prematurely fused, distorting the cranial vault (oxycephaly, trigonocephaly, brachycephaly, plagiocephaly) and faciocraniosynostosis, with facial retrusion (Crouzon, Apert, Pfeiffer, and Saethre-Chozten syndromes). Facial and monobloc distraction is often used for these patients. Since 1992, the pediatricians having recommendedto keep the infants from 0 to 6 months, laying on their back, thenumber of posterior cranial deformations at the wendensly increased.These deformations are positionnal, not synostototic, and can be easilytreated (cf chapter “conditions treated”).  Another group of craniofacial anomalies is represented by facial clefts with hypertelorism, nasal anomalies, palpebral colobomata, encephaloceles, and Treacher-Collins syndrome. Many of these syndromes require complex orbital surgeries, for orbital dystopia. For example, bringing the orbits together in hypertelorism (widely-spaced orbits) requires complete orbital mobilization, such as in transcranial or subcranial facial bipartition. Progressive craniofacial anomalies like neurofibromatosis (Recklinghausen disease) and fibrous dysplasia require complex treatments. Craniofacial techniques are also used for treatment of orbitofrontal fractures and for post-traumatic sequelae, especially malar and ethmoidal fractures.   © 2005 Craniofacial Group Paris France - All rights reserved Craniostenosis, hypertelorism, Crouzon syndrom, Apert syndrom, facial clefts with hypertelorism Facial clefts with hypertelorism, craniostenosis, Apert syndrom, hypertelorism, Crouzon syndrom
 

Craniofacial

Group;

Management

of

anomalies

of

skull

and

face

:

craniosynostosis,

facial

clefts,

hypertelorism,

tumors

and

trauma.


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