A Cephalometric Analysis of Maxillary and Mandibular Parameters in Treacher Collins Syndrome

被引:37
作者
Chong, David K.
Murray, Dylan J.
Britto, Jonathan A.
Tompson, Brian
Forrest, Christopher R.
Phillips, John H. [1 ]
机构
[1] Hosp Sick Children, Div Plast Surg, Ctr Craniofacial Care & Res, Toronto, ON M5G 1X8, Canada
关键词
D O I
10.1097/01.prs.0000299379.64906.2e
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: Treacher Collins syndrome is an autosomal dominant condition of varying severity, affecting the tissues of the first and second branchial arches. The aim of this article is to present a cephalometric analysis of the craniofacial skeleton in Treacher Collins syndrome and provide an age-and sex-matched comparison as a standard control sample. Methods: Twenty-four Treacher Collins syndrome patients (11 male patients and 13 female patients; mean age, 17.99 +/- 1.96 years) underwent cephalometric studies, including orthopantomography and lateral and anteroposterior cephalography, as part of their preparation for bimaxillary surgery. Cephalometric parameters assessing the relationships of the skull base, maxilla, and mandible were analyzed and compared with age-and sex-matched control data (mean age, 17.75 +/- 1.95 years). Results: Cephalometric analysis before orthognathic surgery documented that the Treacher Collins syndrome mandible and midface are expectedly short in the anteroposterior plane; however, the ratio of maxillomandibular deficiency is particularly significant in the female patient. The mandibular plane angle is obtuse, affecting female patients in particular, in whom there is also a posteriorly placed chin point. Affected individuals have a high antegonial notch height. Although the parameters of anterior lower facial height proportion in control and syndrome individuals are similar, posterior face height in Treacher Collins syndrome is reduced. Conclusions: This study quantifies the cephalometric dysmorphology of patients with Treacher Collins syndrome and compares it to that of age-matched controls. These cephalometric characteristics have clinical significance in Treacher Collins syndrome and in the planning of bimaxillary advancement and genioplasty in syndrome patients. (Plast. Reconstr. Surg. 121: 77e, 2008.)
引用
收藏
页码:77E / 84E
页数:8
相关论文
共 23 条
[1]  
ARVYSTAS M, 1991, CLEFT PALATE-CRAN J, V28, P226, DOI 10.1597/1545-1569(1991)028<0226:CMITCS>2.3.CO
[2]  
2
[3]   Adolescents' perspectives on living and growing up with Treacher Collins syndrome: A qualitative study [J].
Beaune, L ;
Forrest, CR ;
Keith, T .
CLEFT PALATE CRANIOFACIAL JOURNAL, 2004, 41 (04) :343-350
[4]   Tcof1/Treacle is required for neural crest cell formation and proliferation deficiencies that cause craniofacial abnormalities [J].
Dixon, Jill ;
Jones, Natalie C. ;
Sandell, Lisa L. ;
Jayasinghe, Sachintha M. ;
Crane, Jennifer ;
Rey, Jean-Philippe ;
Dixon, Michael J. ;
Trainor, Paul A. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (36) :13403-13408
[5]  
Dixon Michael J., 1992, Human Molecular Genetics, V1, P249, DOI 10.1093/hmg/1.4.249
[6]   INTERACTION OF CRANIOFACIAL DYSMORPHOLOGY, GROWTH, AND PREDICTION OF SURGICAL OUTCOME [J].
DUFRESNE, C ;
RICHTSMEIER, JT .
JOURNAL OF CRANIOFACIAL SURGERY, 1995, 6 (04) :270-281
[7]   Prenatal diagnosis in Treacher Collins syndrome using combined linkage analysis and ultrasound imaging [J].
Edwards, SJ ;
Fowlie, A ;
Cust, MP ;
Liu, DTY ;
Young, ID ;
Dixon, MJ .
JOURNAL OF MEDICAL GENETICS, 1996, 33 (07) :603-606
[8]  
FRANCESCHETTI A, 1949, Acta Ophthalmol (Copenh), V27, P143
[9]   Variations in the correction of Treacher Collins syndrome [J].
Freihofer, HPM .
PLASTIC AND RECONSTRUCTIVE SURGERY, 1997, 99 (03) :647-657
[10]  
Garner L D, 1967, J Dent Child, V34, P531