Review of the Genetic Basis of Jaw Malformations

被引:9
作者
Ahmed, Mairaj K. [1 ,2 ]
Ye, Xiaoqian [3 ]
Taub, Peter J. [4 ]
机构
[1] Icahn Sch Med Mt Sinai, Dept Dent Oral & Maxillofacial Surg, New York, NY USA
[2] Icahn Sch Med Mt Sinai, Dept Otolaryngol, New York, NY USA
[3] Icahn Sch Med Mt Sinai, Dept Genet & Genom Sci, New York, NY USA
[4] Icahn Sch Med Mt Sinai, Div Plast & Reconstruct Surg, 5 East 98th St, New York, NY 10029 USA
关键词
malocclusion; mandible; maxilla; congenital; Treacher Collins; mandibulofacial dysostosis; Nager; Miller;
D O I
10.1055/s-0036-1593505
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Genetic etiologies for congenital anomalies of the facial skeleton, namely, the maxilla and mandible, are important to understand and recognize. Malocclusions occur when there exist any significant deviation from what is considered a normal relationship between the upper jaw (maxilla) and the lower jaw (mandible). They may be the result of anomalies of the teeth alone, the bones alone, or both. A number of genes play a role in the facial skeletal development and are regulated by a host of additional regulatory molecules. As such, numerous craniofacial syndromes specifically affect the development of the jaws. The following review discusses several genetic anomalies that specifically affect the bones of the craniofacial skeleton and lead to malocclusion.
引用
收藏
页码:209 / 219
页数:11
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