The role of bone centers in the pathogenesis of craniosynostosis: An embryologic approach using CT measurements in isolated craniosynostosis and Apert and Crouzon syndromes

被引:33
作者
Mathijssen, IMJ [1 ]
Vaandrager, JM [1 ]
vanderMeulen, JC [1 ]
Pieterman, H [1 ]
Zonneveld, FW [1 ]
Kreiborg, S [1 ]
VermeijKeers, C [1 ]
机构
[1] ACAD HOSP ROTTERDAM, DEPT ANAT PLAST & RECONSTRUCT SURG, 3000 DR ROTTERDAM, NETHERLANDS
关键词
D O I
10.1097/00006534-199607000-00004
中图分类号
R61 [外科手术学];
学科分类号
摘要
This paper describes the role of the displacement of bone centers, i.e., the tubers, in the pathogenesis of craniosynostosis. This displacement was studied in 54 patients with isolated or syndromic craniosynostosis in the form of CT scans as well as in two dw neonate skulls with Apert syndrome. For comparison, 49 fetal and 8 normal infant dry skulls were studied. Our investigation was restricted to the coronal and metopic sutures. The results showed a significantly more occipital localization of the frontal bone center and a more frontal localization of the parietal bone center at the side of a synostotic coronal suture in the isolated form as well as in Apert syndrome. In contrast, this was not the case in Crouzon syndrome, thus showing that these two syndromes have a different pathogenesis. For trigonocephaly, a more anteromedial localization of the frontal bone centers was found.
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页码:17 / 26
页数:10
相关论文
共 53 条
[41]   A MORPHOGENETIC CLASSIFICATION OF CRANIOFACIAL MALFORMATIONS [J].
VANDERMEULEN, JC ;
MAZZOLA, R ;
VERMEYKEERS, C ;
STRICKER, M ;
RAPHAEL, B .
PLASTIC AND RECONSTRUCTIVE SURGERY, 1983, 71 (04) :560-572
[42]  
Vermeij-Keers C, 1990, CRANIOFACIAL MALFORM
[43]  
VERMEIJKEERS C, 1983, CLEFT PALATE J, V20, P128
[44]  
WAITZMAN AA, 1992, CLEFT PALATE-CRAN J, V29, P112, DOI 10.1597/1545-1569(1992)029<0112:CSMBOC>2.3.CO
[45]  
2
[46]  
WAITZMAN AA, 1992, CLEFT PALATE-CRAN J, V29, P118, DOI 10.1597/1545-1569(1992)029<0118:CSMBOC>2.3.CO
[47]  
2
[48]   APERT SYNDROME RESULTS FROM LOCALIZED MUTATIONS OF FGFR2 AND IS ALLELIC WITH CROUZON SYNDROME [J].
WILKIE, AOM ;
SLANEY, SF ;
OLDRIDGE, M ;
POOLE, MD ;
ASHWORTH, GJ ;
HOCKLEY, AD ;
HAYWARD, RD ;
DAVID, DJ ;
PULLEYN, LJ ;
RUTLAND, P ;
MALCOLM, S ;
WINTER, RM ;
REARDON, W .
NATURE GENETICS, 1995, 9 (02) :165-172
[49]  
Williams P.L., 1989, GRAYS ANATOMY
[50]  
WRETE M, 1955, KONGENITALEN MISSBIL