Skeletal Malocclusion: A Developmental Disorder With a Life-Long Morbidity
Abstract
 The likelihood of birth defects in orofacial tissues  			is high due to the structural and developmental complexity of the  			face and the susceptibility to intrinsic and extrinsic  			perturbations. Skeletal   malocclusion is caused by the distortion of the proper mandibular  			and/or maxillary growth during fetal development.  Patients with skeletal malocclusion may suffer from dental deformities, bruxism, teeth crowding, trismus, mastication  			difficulties, breathing obstruction and digestion disturbance if the  			problem is left untreated. In this review, we focused on skeletal  			malocclusion that affects 27.9% of the US population with different  			severity levels. We summarized the prevalence of    class I, II and III of malocclusion in different  			ethnic groups and discussed the most frequent medical disorders  			associated with skeletal malocclusion. Dental anomalies that lead to  			malocclusion such as tooth agenesis, crowding, missing teeth and  			abnormal tooth size are not addressed in this review. We propose a  			modified version of malocclusion classification for research  			purposes to exhibit a clear distinction between skeletal vs. dental  			malocclusion in comparison to Angle’s classification. In addition,  			we performed a cross-sectional analysis on orthodontic  			(malocclusion) data through the BigMouth Dental Data Repository   to calculate potential association between  			malocclusion with other medical conditions. In conclusion, this  			review emphasizes the need to identify genetic and environmental  			factors that cause or contribute risk to skeletal malocclusion and  			the possible association with other medical conditions to improve  			assessment, prognosis and therapeutic approaches.
J Clin Med Res. 2014;6(6):399-408
doi: http://dx.doi.org/10.14740/jocmr1905w
		J Clin Med Res. 2014;6(6):399-408
doi: http://dx.doi.org/10.14740/jocmr1905w
Keywords
Skeletal malocclusion; Micrognathia; Retrognathia; Prognathia; Late-onset diseases
		

