Literature DB >> 25686894

Morphology of the foramen magnum in syndromic and non-syndromic brachycephaly.

Reza Assadsangabi1, Mehrdad Hajmomenian, Larissa T Bilaniuk, Arastoo Vossough.   

Abstract

PURPOSE: The shape and size of the foramen magnum (FM) can be altered in craniosynostoses. However, few studies have investigated these changes. In this paper, we investigate the morphology of the foramen magnum in syndromic and non-syndromic brachycephaly.
METHODS: Surface area, anteroposterior (AP) diameter, and transverse diameters of the FM were measured on high-resolution CT scans in children with Crouzon (25), Pfeiffer (21), Apert (26), Saethre-Chotzen (7) syndromes, and isolated bicoronal synostosis (9) and compared to an age-matched control group (30).
RESULTS: A significantly smaller FM surface area was observed in Crouzon (6.3 ± 1.7 cm(2)) and Pfeiffer (6.4 ± 2.3 cm(2)) syndromes as compared to the control group (7.4 ± 1.3 cm(2), p = 0.006 and p = .017, respectively). In comparison to the control group, no statistically significant alteration in FM surface area was noted in patients with Apert, Saethre-Chotzen, or isolated bicoronal synostosis (p = 0.37, p = 0.71, p = 0.40 respectively). The transverse diameter of FM was significantly smaller in Crouzon, Pfeiffer, and Apert syndromes compared to the control group (p = 0.005, p = 0.002, p = 0.03 respectively). In Saethre-Chotzen and isolated bicoronal synostosis, no difference in transverse diameter was demonstrated. Among all groups, only Crouzon syndrome showed reduced anteroposterior diameter as compared to controls (p = 0.005). In Pfeiffer and Apert syndromes, there was elongation of the shape of the FM with a relatively narrowed width as demonstrated in a significantly increased AP to transverse diameter ratio (p = 0.002 and p = 0.019, respectively). DISCUSSION AND
CONCLUSIONS: The FM shape and area is significantly altered in fibroblast growth factor receptor (FGFR)-related brachycephaly syndromes (Crouzon, Pfeiffer, and Apert), whereas in patients with Saethre-Chotzen syndrome (TWIST-1 mutation) and isolated non-syndromic bicoronal synostosis, the shape and mean FM area was not statistically different from that of normals. This study brings to light the important role of FGFRs on FM growth and shape. TWIST-1 mutation (Saethre-Chotzen syndrome) does not appear to have an important effect in shaping the FM.

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Year:  2015        PMID: 25686894     DOI: 10.1007/s00381-015-2639-0

Source DB:  PubMed          Journal:  Childs Nerv Syst        ISSN: 0256-7040            Impact factor:   1.475


  22 in total

1.  Craniosynostosis.

Authors:  R I Aviv; E Rodger; C M Hall
Journal:  Clin Radiol       Date:  2002-02       Impact factor: 2.350

Review 2.  Saethre-Chotzen syndrome: review of the literature and report of a case.

Authors:  L Clauser; M Galiè; A Hassanipour; O Calabrese
Journal:  J Craniofac Surg       Date:  2000-09       Impact factor: 1.046

3.  Premature closure of the spheno-occipital synchondrosis in Pfeiffer syndrome: a link to midface hypoplasia.

Authors:  James Thomas Paliga; Jesse A Goldstein; Arastoo Vossough; Scott P Bartlett; Jesse Adam Taylor
Journal:  J Craniofac Surg       Date:  2014-01       Impact factor: 1.046

Review 4.  Skull base embryology: a multidisciplinary review.

Authors:  Antonio Di Ieva; Emiliano Bruner; Thomas Haider; Luigi F Rodella; John M Lee; Michael D Cusimano; Manfred Tschabitscher
Journal:  Childs Nerv Syst       Date:  2014-04-17       Impact factor: 1.475

5.  Foramen magnum ontogeny in Homo sapiens: a functional matrix perspective.

Authors:  Gary D Richards; Rebecca S Jabbour
Journal:  Anat Rec (Hoboken)       Date:  2010-12-23       Impact factor: 2.064

Review 6.  Skull base growth in craniosynostosis.

Authors:  James Tait Goodrich
Journal:  Childs Nerv Syst       Date:  2005-05-20       Impact factor: 1.475

7.  The spheno-occipital synchondrosis fuses prematurely in patients with Crouzon syndrome and midface hypoplasia compared with age- and gender-matched controls.

Authors:  Youssef Tahiri; J Thomas Paliga; Arastoo Vossough; Scott P Bartlett; Jesse A Taylor
Journal:  J Oral Maxillofac Surg       Date:  2013-11-22       Impact factor: 1.895

8.  Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome.

Authors:  T D Howard; W A Paznekas; E D Green; L C Chiang; N Ma; R I Ortiz de Luna; C Garcia Delgado; M Gonzalez-Ramos; A D Kline; E W Jabs
Journal:  Nat Genet       Date:  1997-01       Impact factor: 38.330

9.  Morphometric comparison of foramen magnum in non-syndromic craniosynostosis patients with or without Chiari I malformation.

Authors:  J Leikola; V Haapamäki; A Karppinen; V Koljonen; J Hukki; L Valanne; M Koivikko
Journal:  Acta Neurochir (Wien)       Date:  2012-08-07       Impact factor: 2.216

10.  The foramen magnum in isolated and syndromic brachycephaly.

Authors:  Federico Di Rocco; Dana Dubravova; Jawad Ziyadeh; Christian Sainte-Rose; Corinne Collet; Eric Arnaud
Journal:  Childs Nerv Syst       Date:  2013-10-18       Impact factor: 1.475

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  3 in total

1.  Morphology of the foramen magnum in syndromic and non-syndromic brachycephaly: letter to the editor.

Authors:  Guillaume Coll; Federico Di Rocco
Journal:  Childs Nerv Syst       Date:  2015-04-18       Impact factor: 1.475

2.  Central nervous system and cervical spine abnormalities in Apert syndrome.

Authors:  Omar Breik; Antony Mahindu; Mark H Moore; Cindy J Molloy; Stephen Santoreneos; David J David
Journal:  Childs Nerv Syst       Date:  2016-02-10       Impact factor: 1.475

3.  The foramen magnum in scaphocephaly.

Authors:  Tymon Skadorwa; Olga Wierzbieniec
Journal:  Childs Nerv Syst       Date:  2022-08-05       Impact factor: 1.532

  3 in total

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