2017
DOI: 10.5937/sejodr3-15218
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Craniofacial morphology in individuals with increasing severity of hypodontia

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Cited by 3 publications
(5 citation statements)
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References 28 publications
(24 reference statements)
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“…tia severity increased, ANB reduced; therefore, it was concluded that patients with hypodontia tended toward a Class III skeletal relationship. 2,9,10,18,26 Meanwhile, Bassiouny et al 30 studied a sample of patients with congenitally missing maxillary lateral incisors and proved them to have a significant tendency to develop a Class III skeletal relationship with reduced ANB and Wits. In the present study, chin protrusion, measured by Pog-NB, was significantly increased in postpubertal patients with hypodontia, indicating that patients with hypodontia appeared to have a more prominent chin.…”
Section: Discussionmentioning
confidence: 99%
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“…tia severity increased, ANB reduced; therefore, it was concluded that patients with hypodontia tended toward a Class III skeletal relationship. 2,9,10,18,26 Meanwhile, Bassiouny et al 30 studied a sample of patients with congenitally missing maxillary lateral incisors and proved them to have a significant tendency to develop a Class III skeletal relationship with reduced ANB and Wits. In the present study, chin protrusion, measured by Pog-NB, was significantly increased in postpubertal patients with hypodontia, indicating that patients with hypodontia appeared to have a more prominent chin.…”
Section: Discussionmentioning
confidence: 99%
“…Craniofacial morphology was described by a customized cephalometric analysis that included the most frequently used cephalometric measurements from previous studies, comprising 10 angular and 7 linear measurements and 2 derived proportions. 1,2,10,18,21,[26][27][28] These measurements covered the maxillary, mandibular, and maxillomandibular skeletal characteristics, vertical relationship, and soft See Table 1 for definitions of measurement.…”
Section: Data Collectionmentioning
confidence: 99%
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“…However, many human and animal studies found that dental anomalies, mainly missing teeth, and craniofacial alterations, could share common genetic factors [39][40][41][42], such as mutations in MSX1, PAX9, TGF-α and FGF family genes [42,43]. Interestingly, some of these genetic mutations were associated with missing specific tooth types.…”
Section: Missing Teethmentioning
confidence: 99%