Orthodontics Diagnosis and Treatment Plans of Craniosynostosis Syndromes, Report of Three Cases

[1]  R. Coletta,et al.  Pfeiffer syndrome: Clinical and genetic findings in five Brazilian families , 2014, Medicina oral, patologia oral y cirugia bucal.

[2]  G. Farronato,et al.  Non surgical treatment of Crouzon syndrome. , 2014, Stomatologija.

[3]  A. Jezela-Stanek,et al.  Genetic causes of syndromic craniosynostoses. , 2013, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

[4]  K. Vargervik,et al.  Craniofacial team management in Apert syndrome. , 2012, American journal of orthodontics and dentofacial orthopedics : official publication of the American Association of Orthodontists, its constituent societies, and the American Board of Orthodontics.

[5]  E. Tanaka,et al.  Long-term stability of LeFort III distraction osteogenesis with a rigid external distraction device in a patient with Crouzon syndrome. , 2011, American journal of orthodontics and dentofacial orthopedics : official publication of the American Association of Orthodontists, its constituent societies, and the American Board of Orthodontics.

[6]  A. Hegde,et al.  Crouzon's syndrome: A review of literature and case report , 2011, Contemporary clinical dentistry.

[7]  C. Maspero,et al.  Eziopatogenesi e manifestazioni cliniche della sindrome di Crouzon: revisione della letteratura , 2010 .

[8]  P. Hlongwa.  Early orthodontic management of Crouzon Syndrome: a case report , 2009, Journal of maxillofacial and oral surgery.

[9]  A. Afzal,et al.  Diagnosis and evaluation of Crouzon syndrome. , 2009, Journal of the College of Physicians and Surgeons--Pakistan : JCPSP.

[10]  I. Mathijssen,et al.  Advancement of the midface, from conventional Le Fort III osteotomy to Le Fort III distraction: review of the literature. , 2008, International journal of oral and maxillofacial surgery.

[11]  J. McCarthy,et al.  Midterm Follow-Up of Midface Distraction for Syndromic Craniosynostosis: A Clinical and Cephalometric Study , 2007, Plastic and reconstructive surgery.

[12]  U. Joos,et al.  The spectrum of Apert syndrome: phenotype, particularities in orthodontic treatment, and characteristics of orthognathic surgery , 2007, Head & face medicine.

[13]  A. Hackett,et al.  FGFR1 Pfeiffer syndrome without craniosynostosis: an additional case report , 2006, Clinical dysmorphology.

[14]  J. Phillips,et al.  Le Fort III Osteotomy or Distraction Osteogenesis Imperfecta: Your Choice , 2006, Plastic and reconstructive surgery.

[15]  T. Meling,et al.  Le Fort III Distraction Osteogenesis in Syndromal Craniosynostosis , 2006, The Journal of craniofacial surgery.

[16]  A. Bozzetti,et al.  Le Fort III Advancement Osteotomy in the Growing Child Affected by Crouzon's and Apert's Syndromes: Presurgical and Postsurgical Growth , 2005, The Journal of craniofacial surgery.

[17]  J. Fearon.  Halo Distraction of the Le Fort III in Syndromic Craniosynostosis: A Long-Term Assessment , 2005, Plastic and reconstructive surgery.

[18]  A. Scalise,et al.  From the “Charretera” to the Supraclavicular Fascial Island Flap: Revisitation and Further Evolution of a Controversial Flap , 2005, Plastic and reconstructive surgery.

[19]  J. McCarthy,et al.  Understanding the Molecular Basis of Apert Syndrome , 2005, Plastic and reconstructive surgery.

[20]  C. Nurko,et al.  Dental and orthodontic management of patients with Apert and Crouzon syndromes. , 2004, Oral and maxillofacial surgery clinics of North America.

[21]  K. Moriyama,et al.  Segmental distraction of the midface in a patient with Crouzon syndrome. , 2002, The Journal of craniofacial surgery (Print).

[22]  J. Fearon.  The Le Fort III Osteotomy: To Distract or Not to Distract? , 2001, Plastic and reconstructive surgery.

[23]  J. Posnick,et al.  The craniofacial dysostosis syndromes: current surgical thinking and future directions. , 2000, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

[24]  J. A. Harris,et al.  Birth prevalence, mutation rate, sex ratio, parents' age, and ethnicity in Apert syndrome. , 1997, American journal of medical genetics.

[25]  A. Figueroa,et al.  Management of severe maxillary deficiency in childhood and adolescence through distraction osteogenesis with an external, adjustable, rigid distraction device. , 1997, The Journal of craniofacial surgery.

[26]  K. Vargervik,et al.  Dental development in Apert syndrome. , 1997, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

[27]  A. Kuijpers-Jagtman,et al.  Maxillary and Mandibular Dental-Arch Dimensions and Occlusion in Bilateral Cleft Lip and Palate Patients from 3 to 17 Years of Age , 1997, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

[28]  J. Posnick.  The craniofacial dysostosis syndromes. Current reconstructive strategies. , 1994, Clinics in plastic surgery.

[29]  S. Kreiborg,et al.  New indirect method for estimating the birth prevalence of the Apert syndrome. , 1992, International journal of oral and maxillofacial surgery.

[30]  J. Posnick,et al.  Craniofacial skeletal measurements based on computed tomography: Part II. Normal values and growth trends. , 1992, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

[31]  F. Bookstein,et al.  The Le Fort III Advancement Osteotomy in the Child under 7 Years of Age , 1990, Plastic and reconstructive surgery.

[32]  T. Vecchione.  Glabellar Frown Lines: Direct Excision, An Evaluation of the Scars , 1990, Plastic and Reconstructive Surgery.