Utilization of three-dimensional computed tomography for craniofacial phenotypic analysis in children with velocardiofacial syndrome

Journal of Craniofacial Surgery

Volumn 20, Issue 6, 2009, Pages 2013-2019

  Wang, Ke ^a   Yang, Yusheng ^a   Shen, Fang ^b   Tao, Jiang ^b   Xu, Haisong ^a   Portnof, Jason E ^a   Wang, Guomin ^a   Salyer, Kenneth E ^c  

^a SHANGHAI JIAO TONG UNIVERSITY SCHOOL OF MEDICINE   (China)

^b QINGDAO UNIVERSITY   (China)

^c ROYAL CHILDREN'S HOSPITAL   (Australia)

Author keywords

Craniofacial; Three dimensional measurement; Velocardiofacial syndrome

Indexed keywords

ADOLESCENT; ARTICLE; CASE CONTROL STUDY; CEPHALOMETRY; CHILD; CHROMOSOME 22; CROSS-SECTIONAL STUDY; DIGEORGE SYNDROME; EVALUATION; FEMALE; GENE DELETION; GENETICS; HARD PALATE; HUMAN; MALE; METHODOLOGY; PALATOPHARYNGEAL INCOMPETENCE; PATHOLOGY; PHENOTYPE; RADIOGRAPHY; RETROSPECTIVE STUDY; SPIRAL COMPUTER ASSISTED TOMOGRAPHY; THREE DIMENSIONAL IMAGING; TOOTH OCCLUSION; TOOTH RADIOGRAPHY; UTILIZATION REVIEW;

ADOLESCENT; CASE-CONTROL STUDIES; CEPHALOMETRY; CHILD; CHROMOSOMES, HUMAN, PAIR 22; CROSS-SECTIONAL STUDIES; DIGEORGE SYNDROME; FEMALE; HUMANS; IMAGING, THREE-DIMENSIONAL; MALE; PALATE, HARD; PHENOTYPE; RADIOGRAPHY, DENTAL, DIGITAL; RETROSPECTIVE STUDIES; SEQUENCE DELETION; TOMOGRAPHY, SPIRAL COMPUTED; VELOPHARYNGEAL INSUFFICIENCY; VERTICAL DIMENSION;

EID: 77449140636     PISSN: 10492275     EISSN: 15363732     Source Type: Journal    
DOI: 10.1097/SCS.0b013e3181bd2e34     Document Type: Article

References (14)

1. Yamagishi H, Srivastava D. Unraveling the genetic and developmental mysteries of 22q11 deletion syndrome. Trends Mol Med 2003;9:383-389
2. Shprintzen RJ, Higgins AM, Antshel K, et al. Velo-cardio-facial syndrome. Curr Opin Pediatr 2005;17:725-730
3. Shprintzen RJ. Velo-cardio-facial syndrome: 30 years of study. Dev Disabil Res Rev 2008;14:3-10
4. Kobrynski LJ, Sullivan KE. Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes. Lancet 2007;370:1443-1452
5. Cuneo BF. 22q11.2 deletion syndrome: DiGeorge, velocardiofacial, and conotruncal anomaly face syndromes. Curr Opin Pediatr 2001;13:465-472
6. Akcakus M, Ozkul Y, Gunes T, et al. Associated anomalies in asymmetric crying facies and 22q11 deletion. Genet Couns 2003;14:325-330
7. Weinberg SM, Naidoo S, Govier DP, et al. Anthropometric precision and accuracy of digital three-dimensional photogrammetry: comparing the Genex and 3dMD imaging systems with one another and with direct anthropometry. J Craniofac Surg 2006;17:477-483
8. Allanson JE, Hennekam RC. Rubinstein-Taybi syndrome: objective evaluation of craniofacial structure. Am J Med Genet. 1997;71:414-419
9. Ward RE, Jamison PL, Allanson JE. Quantitative approach to identifying abnormal variation in the human face exemplified by a study of 278 individuals with five craniofacial syndromes. Am J Med Genet 2000;91:8-17
10. Ferrario VF, Dellavia C, Serrao G, et al. Soft tissue facial angles in Down's syndrome subjects: a three-dimensional non-invasive study. Eur J Orthod 2005;27:355-362
11. Meintjes EM, Douglas TS, Martinez F, et al. A stereo-photogrammetric method to measure the facial dysmorphology of children in the diagnosis of fetal alcohol syndrome. Med Eng Phys 2002;24:683-689
12. Guyot L, Dubuc M, Pujol J, et al. Craniofacial anthropometric analysis in patients with 22q11 microdeletion. Am J Med Genet 2001;100:1-8
13. Ruotolo RA, Veitia NA, Corbin A, et al. Velopharyngeal anatomy in 22q11.2 deletion syndrome: a three-dimensional cephalometric analysis. Cleft Palate Craniofac J 2006;43:446-456
14. Kim NK, Lee C, Kang SH, et al. A three-dimensional analysis of soft and hard tissue changes after a mandibular setback surgery. Comput Methods Programs Biomed 2006.83:87