Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
1994-7-25
pubmed:abstractText
The incidence of premature craniosynostosis is 1:2000-1:4000. Ninety percent of these are simple synostosis with premature closure of one or more of the cranial sutures causing reduced or arrested growth perpendicular to the closed suture(s). Ten percent are more complex craniofacial syndromes, where hypoplasia of the maxilla is also of importance to the development of the orbits. The reduced intracranial volume may result in an increased intracranial pressure and is a contributing factor to the rather high frequency of mental retardation seen in patients with premature craniosynostosis. Early correction is necessary in order to achieve a satisfactory cosmetic result as well as prevention of secondary damage to the brain. Craniofacial syndromes with facial hypoplasia require a staged multi-disciplinary treatment. Patients with simple craniosynostosis have to be treated within the first six months after birth.
pubmed:language
dan
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0041-5782
pubmed:author
pubmed:issnType
Print
pubmed:day
7
pubmed:volume
156
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1459-65
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed:year
1994
pubmed:articleTitle
[Premature craniosynostosis. Diagnosis and treatment].
pubmed:affiliation
Arhus Kommunehospital, neurokirurgisk afdeling.
pubmed:publicationType
Journal Article, English Abstract, Review, Research Support, Non-U.S. Gov't