2012
DOI: 10.5005/jp-journals-10024-1218
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Orthodontic and Surgical Treatment of a Patient with Apert Syndrome

Abstract: The aim of this case report was to present the combined orthodontic and surgical treatment of a patient with Apert syndrome in an adult stage. A 15 years old male patient with Apert syndrome was concerned about the appearance of his face and malocclusion. His profile was concave with a retruded maxilla and prominent lower lip. He had an Angle class I molar relationship with a 9.5 mm anterior open bite. The amount of crowding was 20.4 mm in the maxilla and 6 mm in the mandible. Cephalometric analysis revealed a… Show more

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Cited by 4 publications
(3 citation statements)
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“…As the child attains school age a psychological evaluation can be scheduled to detect and institute an intervention plan targeting cognitive/academic skills, language, and/or social-emotional development problems [ 2 ]. Management of physical deformities is preferably started during childhood, but if this is not done then later orthodontic and surgical treatments can be offered to an adult patient like our case [ 12 ].…”
Section: Discussionmentioning
confidence: 99%
“…As the child attains school age a psychological evaluation can be scheduled to detect and institute an intervention plan targeting cognitive/academic skills, language, and/or social-emotional development problems [ 2 ]. Management of physical deformities is preferably started during childhood, but if this is not done then later orthodontic and surgical treatments can be offered to an adult patient like our case [ 12 ].…”
Section: Discussionmentioning
confidence: 99%
“…If possible, physical deformity management should begin in childhood; nonetheless, adult patients may have orthodontic and surgical therapy in the future [32]. Surgical correction of the craniofacial region and fingers and toes may result in considerable functional and aesthetic improvement when diagnosed in the patient as early as three months of age.…”
Section: Medical Managementmentioning
confidence: 99%
“…Specifically, the FGFR2 gene is linked to Crouzon syndrome and Apert syndrome, which cause midface hypoplasia, a high-arched palate, and malocclusions, including AOB. 31 , 32 Another gene that may cause AOB is the TCOF1 gene associated with Treacher–Collins syndrome, a genetic disorder characterized by micrognathia, cleft palate, and other craniofacial anomalies. 33 Additionally, in certain rare hereditary diseases, such as trichorhinophalangeal syndrome linked to the TRPS1 gene, AOB malocclusion is a common clinical manifestation.…”
Section: Introductionmentioning
confidence: 99%