Literature DB >> 2074277

Characteristics of the infant Apert skull and its subsequent development.

S Kreiborg1, M M Cohen.   

Abstract

The purpose of the paper is to describe and analyze the infant Apert skull with emphasis on the calvaria and its early postnatal development. Skull radiographs of 16 Apert syndrome patients were examined (12 American, 4 Danish; 8 males, 8 females). The criterion for inclusion in the study was that the first skull film had to be obtained before 1 year of age. Study methods employed included plain skull radiographs, roentgencephalometric films in several projections, CT-scans, and 3-D reconstructions. Data from 2 dry skulls and 2 early cases from the literature were also evaluated The following findings were common to all cases during early infancy (less than 3 months): The coronal suture area was prematurely closed and was represented by a bone condensation line beginning at the cranial base, extending upwards, and having a characteristic posterior convexity. Anterior and posterior fontanelles were widely patent. The midline of the calvaria had a gaping defect which extended from the glabellar area to the posterior fontanelle via the metopic suture area, anterior fontanelle, and sagittal suture area. Bony islands of varying sizes were observed in the midline defect. The calvaria was hypomineralized. During the first 2-4 years of life, the midline defect was obliterated by coalescence of the enlarging bony islands without evidence of any proper formation of sutures. The calvaria became thicker with time and several cases developed increased digital markings and enlargement of the sella turcica. During infancy, the Apert skull with its gaping midline defect appears to permit adequate accommodation of the growing brain, albeit distorted in shape. Normal metopic, sagittal, and coronal sutures with interdigitations were not observed in a single instance; in contrast, the lambdoidal sutures appeared normal in all cases. The invariable findings of an extremely short squama and orbital part of the frontal bone together with the posterior convexity of the coronal bone condensation line suggest that growth inhibition in the sphenofrontal and coronal suture area has its onset very early in fetal life.

Entities:  

Mesh:

Year:  1990        PMID: 2074277

Source DB:  PubMed          Journal:  J Craniofac Genet Dev Biol        ISSN: 0270-4145


  8 in total

1.  Cranio-maxillofacial, orthodontic and dental treatment in three patients with Apert syndrome.

Authors:  S Carpentier; J Schoenaers; C Carels; A Verdonck
Journal:  Eur Arch Paediatr Dent       Date:  2014-03-19

2.  Dynamic morphological changes in the skulls of mice mimicking human Apert syndrome resulting from gain-of-function mutation of FGFR2 (P253R).

Authors:  Xiaolan Du; Tujun Weng; Qidi Sun; Nan Su; Zhi Chen; Huabing Qi; Ming Jin; Liangjun Yin; Qifen He; Lin Chen
Journal:  J Anat       Date:  2010-06-17       Impact factor: 2.610

3.  Craniosynostosis: To Study the Spectrum and Outcome of Surgical Intervention at a Tertiary Referral Institute in India.

Authors:  Charandeep S Gandhoke; Simran K Syal; Ajay Sharma; Arvind K Srivastava; Daljit Singh
Journal:  J Pediatr Neurosci       Date:  2020-06-27

4.  Postnatal brain and skull growth in an Apert syndrome mouse model.

Authors:  Cheryl A Hill; Neus Martínez-Abadías; Susan M Motch; Jordan R Austin; Yingli Wang; Ethylin Wang Jabs; Joan T Richtsmeier; Kristina Aldridge
Journal:  Am J Med Genet A       Date:  2013-03-12       Impact factor: 2.802

5.  Early onset of craniosynostosis in an Apert mouse model reveals critical features of this pathology.

Authors:  Greg Holmes; Gerson Rothschild; Upal Basu Roy; Chu-Xia Deng; Alka Mansukhani; Claudio Basilico
Journal:  Dev Biol       Date:  2009-01-29       Impact factor: 3.582

6.  Unilateral Coronal Craniosynostosis in an Apert-Like Patient.

Authors:  Navid Pourtaheri; Derek Z Wang; Robert P Lesko; Christopher M Bonfield; Peter Taub; Anand R Kumar
Journal:  Plast Surg (Oakv)       Date:  2018-10-03       Impact factor: 0.947

7.  Classification of Subtypes of Apert Syndrome, Based on the Type of Vault Suture Synostosis.

Authors:  Xiaona Lu; Rajendra Sawh-Martinez; Antonio Jorge Forte; Robin Wu; Raysa Cabrejo; Alexander Wilson; Derek M Steinbacher; Michael Alperovich; Nivaldo Alonso; John A Persing
Journal:  Plast Reconstr Surg Glob Open       Date:  2019-03-20

8.  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

  8 in total

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