Results 151 to 160 of about 2,319 (218)

Molecular and Cellular Bases of Syndromic Craniosynostoses

Expert Reviews in Molecular Medicine, 2003
Premature fusion of cranial sutures underlies the clinical condition of ‘craniosynostosis’, a common human disorder that occurs in both nonsyndromic and syndromic forms. The subgroup of syndromic craniosynostoses usually associates limb abnormalities and facial dysmorphism to skull distortion.
Jacky Bonaventure
exaly   +5 more sources

Management of Non-Syndromic Craniosynostoses in France in 2015: A National Survey

Journal of Cranio-Maxillo-Facial Surgery, 2019
PURPOSE Craniosynostoses are managed by surgical and anaesthetic teams in specialist centres. Despite the availability of international guidelines, the perioperative management of craniosynostoses remains highly variable between centres.
Pierre Keribin, Alexis Veyssière, Hervé Benateau   +2 more
exaly   +3 more sources

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Management of Craniosynostoses

Child's Nervous System, 2000
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 ...
Daniel Marchac, Elisabeth Lajeunie, E Arnaud   +2 more
exaly   +3 more sources

Advances in the management of the craniosynostoses

ANZ Journal of Surgery, 2003
The spectacular beginning of craniofacial surgery in the modern era involved a case of craniosynostosis. Progress from that time to the present in the development of our understanding of this disease process and its management reflects the wider progress in the development and institutionalization of the discipline of craniofacial surgery.
David, D.
openaire   +4 more sources

Craniosynostoses

Genetic Consultations in the Newborn, 2019
This chapter reviews background information about the incidence, risk factors, genetics, recurrence risk, and epidemiology of single suture and multiple suture craniosynostosis including isolated and syndromic varieties.
R. Clark, C. Curry
semanticscholar   +2 more sources

Craniosynostoses: Phenotypic/Molecular Correlations

American Journal of Medical Genetics, Part A, 1995
From the discovery of the first known human homeobox mutation in MSX2 for craniosynostosis of the Boston type by Jams to the recent report of 2 mutations in FGFR2 in Apert syndrome by Wilkie, it is clear that the molecular aspects of syndromes with craniosynostosis are becoming known at a dizzying pace. Four of the syndromes involve mutations in FGFR2.
M Michael Cohen, M M Cohen
exaly   +3 more sources

Visual Surveillance in Craniosynostoses

American Orthoptic Journal, 2014
Craniosynostosis is the premature fusion of one or more cranial sutures that may be isolated or syndromic. These children can have multiple developmental issues including speech, hearing, and vision, in addition to the aesthetic issue of an abnormally shaped skull and midfacial hypoplasia. As the aesthetic outcomes of craniofacial surgery have improved,
K. Nischal
semanticscholar   +3 more sources

Maximizing the Functional Benefits of Posterior Calvarial Vault Distraction in Syndromic Craniosynostoses: A Nuanced Approach to Volume, Vein, Vector, and the Vexed Challenge of Functional Outcome in Craniosynostoses

Child's Nervous System
Suhas Udayakumaran
exaly   +2 more sources