Literature DB >> 11151714

Management of craniosynostoses.

D Renier1, E Lajeunie, E Arnaud, D Marchac.   

Abstract

Although it is currently thought that surgery is indicated mainly for cosmetic reasons in isolated craniosynostoses, the functional aspects of the treatment must not be underestimated. Prospective studies on intracranial pressure and mental evolution of these children have shown that there were functional consequences in a significant proportion of cases even of single suture fusion. The frequency of increased intracranial hypertension and the risk of mental impairment depend on the age of the child and the type of craniosynostosis. In nonsyndromic cases, the higher risks are observed in multisutural craniosynostoses (brachycephaly, oxycephaly). In syndromic cases, the risk of intracranial hypertension is higher in Crouzon syndrome, and Apert syndrome carries the higher risk of mental retardation. The study of a personal series of 2,137 craniosynostoses shows that the functional and the cosmetic results are better after early surgery, and that the operative risks are not higher in infants than in older children.

Entities:  

Mesh:

Year:  2000        PMID: 11151714     DOI: 10.1007/s003810000320

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


  76 in total

1.  The prevalence of strabismus in unilateral coronal synostosis.

Authors:  Fares Samra; J Thomas Paliga; Youssef Tahiri; Linton A Whitaker; Scott P Bartlett; Brian J Forbes; Jesse A Taylor
Journal:  Childs Nerv Syst       Date:  2014-11-16       Impact factor: 1.475

2.  Posterior calvarial augmentation in premature craniosynostosis: a technique avoiding foreign implants or free bone flaps.

Authors:  Wolfgang Wagner; Eike Schwandt; Alexandra Huthmann; Sonja Vulcu; Christoph Tschan
Journal:  Childs Nerv Syst       Date:  2010-05-02       Impact factor: 1.475

3.  About the operative management and post-operative neural development of patients with cloverleaf skull deformity.

Authors:  Matthias Preuss; Marco Stein; Bernd A Neubauer; Heidrun Schaaf; Hans-Peter Howaldt; Ulf Nestler; Petros Christophis
Journal:  Childs Nerv Syst       Date:  2010-03-26       Impact factor: 1.475

4.  Guideline for Care of Patients With the Diagnoses of Craniosynostosis: Working Group on Craniosynostosis.

Authors:  Irene M J Mathijssen
Journal:  J Craniofac Surg       Date:  2015-09       Impact factor: 1.046

Review 5.  Craniosynostosis as a clinical and diagnostic problem: molecular pathology and genetic counseling.

Authors:  Anna Kutkowska-Kaźmierczak; Monika Gos; Ewa Obersztyn
Journal:  J Appl Genet       Date:  2018-02-01       Impact factor: 3.240

6.  Apert syndrome without craniosynostosis.

Authors:  Diego de Ângelis Ramos; Hamilton Matushita; Daniel Dante Cardeal; Clarissa Nóbrega Gambarra Nascimento; Manoel Jacobsen Teixeira
Journal:  Childs Nerv Syst       Date:  2019-01-14       Impact factor: 1.475

7.  Effectiveness of a limited invasive scalp approach in the correction of sagittal craniosynostosis.

Authors:  Luca Massimi; Gianpiero Tamburrini; Massimo Caldarelli; Concezio Di Rocco
Journal:  Childs Nerv Syst       Date:  2007-09-18       Impact factor: 1.475

8.  Endoscope-assisted repair of metopic synostosis.

Authors:  Yusuf Erşahin
Journal:  Childs Nerv Syst       Date:  2013-10-03       Impact factor: 1.475

9.  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

10.  Unique modulation of cadherin expression pattern during posterior frontal cranial suture development and closure.

Authors:  David E Sahar; Björn Behr; Kenton D Fong; Michael T Longaker; Natalina Quarto
Journal:  Cells Tissues Organs       Date:  2009-12-24       Impact factor: 2.481

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.