textabstractObjective: Le Fort III osteotomy with distraction osteogenesis (DO) is used to improve the retruded midface in patients with Crouzon or Apert syndrome. This study aimed to evaluate sagittal and vertical preoperative and postoperative cephalometric changes of DO of the midface in patients with Crouzon or Apert syndrome. Design: Population-based case-control study. Patients and Methods: Records of patients with the syndrome of Crouzon (N=6) or Apert (N= 7) were compared, before and after Le Fort III DO, with a nonsyndromic untreated control group (N = 486). Main Outcome Measures: Sagittal and vertical cephalometric maxillary landmarks and measurements were used to predict and measure midface advancement and rotation after Le Fort ...
Objective: To evaluate vertical and sagittal facial growth in children with Apert and Crouzon syndro...
Objective: To evaluate vertical and sagittal facial growth in children with Apert and Crouzon syndro...
Seven patients with craniosynostosis (mean age 8 years, Apert syndrome, n = 4, Crouzon's disease, n ...
Objective: Le Fort III osteotomy with distraction osteogenesis (DO) is used to improve the retruded ...
Objective: Le Fort III osteotomy with distraction osteogenesis (DO) is used to improve the retruded ...
PURPOSE: Rigid external distraction osteogenesis is regarded as a standard treatment for congenital ...
The LeFort III osteotomy is the surgical treatment performed in patients with mid-facial retrusions ...
A retrospective study on the stability of Le Fort III midface advancement with distraction in cranio...
A major concern in FGFR2 craniofaciosynostosis is oculo-orbital disproportion, such that orbital mal...
Cranial deformities often require major surgical procedures to be corrected. Plastic surgeon Paul Te...
Cranial deformities often require major surgical procedures to be corrected. Plastic surgeon Paul Te...
Cranial deformities often require major surgical procedures to be corrected. Plastic surgeon Paul Te...
Crouzon syndrome (CS) is the most common craniosynostosis syndrome and requires a comprehensive mana...
INTRODUCTION: Children with Apert syndrome have hypertelorism and midfacial hypoplasia, which can be...
Objective: To evaluate vertical and sagittal facial growth in children with Apert and Crouzon syndro...
Objective: To evaluate vertical and sagittal facial growth in children with Apert and Crouzon syndro...
Objective: To evaluate vertical and sagittal facial growth in children with Apert and Crouzon syndro...
Seven patients with craniosynostosis (mean age 8 years, Apert syndrome, n = 4, Crouzon's disease, n ...
Objective: Le Fort III osteotomy with distraction osteogenesis (DO) is used to improve the retruded ...
Objective: Le Fort III osteotomy with distraction osteogenesis (DO) is used to improve the retruded ...
PURPOSE: Rigid external distraction osteogenesis is regarded as a standard treatment for congenital ...
The LeFort III osteotomy is the surgical treatment performed in patients with mid-facial retrusions ...
A retrospective study on the stability of Le Fort III midface advancement with distraction in cranio...
A major concern in FGFR2 craniofaciosynostosis is oculo-orbital disproportion, such that orbital mal...
Cranial deformities often require major surgical procedures to be corrected. Plastic surgeon Paul Te...
Cranial deformities often require major surgical procedures to be corrected. Plastic surgeon Paul Te...
Cranial deformities often require major surgical procedures to be corrected. Plastic surgeon Paul Te...
Crouzon syndrome (CS) is the most common craniosynostosis syndrome and requires a comprehensive mana...
INTRODUCTION: Children with Apert syndrome have hypertelorism and midfacial hypoplasia, which can be...
Objective: To evaluate vertical and sagittal facial growth in children with Apert and Crouzon syndro...
Objective: To evaluate vertical and sagittal facial growth in children with Apert and Crouzon syndro...
Objective: To evaluate vertical and sagittal facial growth in children with Apert and Crouzon syndro...
Seven patients with craniosynostosis (mean age 8 years, Apert syndrome, n = 4, Crouzon's disease, n ...