Literature DB >> 3442299

Comparative study of normal, Crouzon, and Apert craniofacial morphology using finite element scaling analysis.

J T Richtsmeier1.   

Abstract

Finite element scaling analysis is used to study differences in morphology between the craniofacial complex of normal individuals and those affected with the syndromes of Apert and Crouzon. Finite element scaling quantifies the differences in shape and size between forms without reference to any fixed, arbitrary registration point or orientation line and measures the amount of form change required to deform one object into another. Two-dimensional coordinates of landmarks digitized from annual sets of cephalometric radiographs were used in the analysis. A simple tabulation shows no difference in variances between the normal and pathological samples. A test of mean differences depicts the Apert and Crouzon morphologies as significantly different from normal. The Apert palate differs from normal in shape in the older age groups analyzed, and palatal size differences are most common at the posterior nasal spine. The Apert pituitary fossa and basi-occiput are significantly larger than normal. The Crouzon pituitary fossa is also larger than normal, but the difference is not always significant. The typical morphology of the Crouzon nose is due more to differences in shape than size. The Crouzon basi-occiput is significantly smaller than normal. An age association of the differences between the normal and pathological craniofacies was found in Apert syndrome but not in Crouzon syndrome. Apert syndrome is characterized by a more homogeneous pattern of craniofacial dysmorphology from 6 months to 18 years of age than Crouzon syndrome.

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Year:  1987        PMID: 3442299     DOI: 10.1002/ajpa.1330740407

Source DB:  PubMed          Journal:  Am J Phys Anthropol        ISSN: 0002-9483            Impact factor:   2.868


  6 in total

1.  Amelioration of Chiari type 1 malformation and syringomyelia following posterior calvarial distraction in Crouzon's syndrome--a case report.

Authors:  Fateh Ahmad; Martin Evans; Nicholas White; Hiroshi Nishikawa; Stephen Dover; Guirish Solanki; Desiderio Rodrigues
Journal:  Childs Nerv Syst       Date:  2013-06-19       Impact factor: 1.475

Review 2.  Chiari malformation in craniosynostosis.

Authors:  Giuseppe Cinalli; Pietro Spennato; Christian Sainte-Rose; Eric Arnaud; Ferdinando Aliberti; Francis Brunelle; Emilio Cianciulli; Dominique Renier
Journal:  Childs Nerv Syst       Date:  2005-05-05       Impact factor: 1.475

3.  Computational mouse atlases and their application to automatic assessment of craniofacial dysmorphology caused by the Crouzon mutation Fgfr2(C342Y).

Authors:  Hildur Olafsdóttir; Tron A Darvann; Nuno V Hermann; Estanislao Oubel; Bjarne K Ersbøll; Alejandro F Frangi; Per Larsen; Chad A Perlyn; Gillian M Morriss-Kay; Sven Kreiborg
Journal:  J Anat       Date:  2007-06-06       Impact factor: 2.610

4.  A genomewide linkage scan for quantitative trait loci influencing the craniofacial complex in baboons (Papio hamadryas spp.).

Authors:  Richard J Sherwood; Dana L Duren; Lorena M Havill; Jeff Rogers; Laura A Cox; Bradford Towne; Michael C Mahaney
Journal:  Genetics       Date:  2008-08-30       Impact factor: 4.562

Review 5.  Functional and morphological changes in hypoplasic posterior fossa.

Authors:  Federico Bianchi; Alberto Benato; Paolo Frassanito; Gianpiero Tamburrini; Luca Massimi
Journal:  Childs Nerv Syst       Date:  2021-06-25       Impact factor: 1.475

6.  Craniofacial divergence by distinct prenatal growth patterns in Fgfr2 mutant mice.

Authors:  Susan M Motch Perrine; Theodore M Cole; Neus Martínez-Abadías; Kristina Aldridge; Ethylin Wang Jabs; Joan T Richtsmeier
Journal:  BMC Dev Biol       Date:  2014-02-28       Impact factor: 1.978

  6 in total

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