OBJECTIVES: To determine whether the midface of patients with Muenke syndrome, Saethre-Chotzen syndrome, or TCF12-related craniosynostosis is hypoplastic compared to skeletal facial proportions of a Dutch control group. MATERIAL AND METHODS: We included seventy-four patients (43 patients with Muenke syndrome, 22 patients with Saethre-Chotzen syndrome, and 9 patients with TCF12-related craniosynostosis) who were referred between 1990 and 2020 (age range 4.84 to 16.83 years) and were treated at the Department of Oral Maxillofacial Surgery, Special Dental Care and Orthodontics, Children's Hospital Erasmus University Medical Center, Sophia, Rotterdam, the Netherlands. The control group consisted of 208 healthy children. RESULTS: Cephalometric v...
Introduction: Apert, Crouzon, and Pfeiffer syndromes are common genetic syndromes related to syndrom...
Objective: To investigate craniofacial characteristics in pediatric patients with Prader–Willi syndr...
Background Prader–Willi syndrome (PWS) is a complex multisystem genetic disorder wit...
Objectives: To determine whether dental maturity (dental development) was delayed in patients with M...
In this case report, we focus on Muenke syndrome (MS), a disease caused by the p.Pro250Arg variant i...
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...
textabstractIn this thesis, one of the most frequently occurring and most variable craniosynostosis ...
Objective: To evaluate vertical and sagittal facial growth in children with Apert and Crouzon syndro...
Aim: To describe the particular craniofacial characteristics of Van der Woude syndrome(VWS) patients...
Introduction: Growth of the facial skeleton is integrated to growth of the cranial base. This relati...
Objective: To quantify soft tissue facial asymmetry (FA) in children with nonsyndromic and Muenke sy...
Objective: To quantify soft tissue facial asymmetry (FA) in children with nonsyndromic and Muenke sy...
Introduction: Apert, Crouzon, and Pfeiffer syndromes are common genetic syndromes related to syndrom...
Introduction: Apert, Crouzon, and Pfeiffer syndromes are common genetic syndromes related to syndrom...
Introduction: Apert, Crouzon, and Pfeiffer syndromes are common genetic syndromes related to syndrom...
Objective: To investigate craniofacial characteristics in pediatric patients with Prader–Willi syndr...
Background Prader–Willi syndrome (PWS) is a complex multisystem genetic disorder wit...
Objectives: To determine whether dental maturity (dental development) was delayed in patients with M...
In this case report, we focus on Muenke syndrome (MS), a disease caused by the p.Pro250Arg variant i...
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...
textabstractIn this thesis, one of the most frequently occurring and most variable craniosynostosis ...
Objective: To evaluate vertical and sagittal facial growth in children with Apert and Crouzon syndro...
Aim: To describe the particular craniofacial characteristics of Van der Woude syndrome(VWS) patients...
Introduction: Growth of the facial skeleton is integrated to growth of the cranial base. This relati...
Objective: To quantify soft tissue facial asymmetry (FA) in children with nonsyndromic and Muenke sy...
Objective: To quantify soft tissue facial asymmetry (FA) in children with nonsyndromic and Muenke sy...
Introduction: Apert, Crouzon, and Pfeiffer syndromes are common genetic syndromes related to syndrom...
Introduction: Apert, Crouzon, and Pfeiffer syndromes are common genetic syndromes related to syndrom...
Introduction: Apert, Crouzon, and Pfeiffer syndromes are common genetic syndromes related to syndrom...
Objective: To investigate craniofacial characteristics in pediatric patients with Prader–Willi syndr...
Background Prader–Willi syndrome (PWS) is a complex multisystem genetic disorder wit...