Unbound MEDLINE

Neurodevelopment of infants with single-suture craniosynostosis: presurgery comparisons with case-matched controls. Plastic and reconstructive surgery [Plast Reconstr Surg] Journal article

 
TitleNeurodevelopment of infants with single-suture craniosynostosis: presurgery comparisons with case-matched controls.
Author(s)Speltz ML, Kapp-Simon K, Collett B, Keich Y, Gaither R, Cradock MM, Buono L, Cunningham ML 
InstitutionDepartment of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA, USA. mspeltz@u.washington.edu
SourcePlast Reconstr Surg 2007 May; 119(6):1874-81.
MeSHCase-Control Studies
Child Behavior Disorders
Child, Preschool
Cranial Sutures
Craniosynostoses
Craniotomy
Developmental Disabilities
Female
Follow-Up Studies
Humans
Incidence
Infant
Male
Neuropsychological Tests
Postoperative Complications
Postoperative Period
Preoperative Care
Probability
Reference Values
Risk Assessment
Suture Techniques
AbstractBACKGROUND: The hypothesized association between single-suture craniosynostosis and neurodevelopment remains unclear, given the methodologic limitations of previous studies, most notably the absence of control groups.
METHODS: Standardized measures were used to assess the neurodevelopment of 125 matched case-control pairs shortly after cases were first diagnosed with isolated fusions of the sagittal, metopic, lambdoid, or right or left coronal sutures. Participants varied in age from 2 to 24 months.
RESULTS: Cases had significantly lower mean standardized scores than controls on measures of cognitive ability and motor functioning (p < 0.02). These differences were unaffected by the location of synostosis, age of diagnosis, infant sex, and maternal IQ. Measures of early language functions revealed no group differences.
CONCLUSIONS: Before cranioplasty, single-suture craniosynostosis is associated with modest but reliable neurodevelopmental delays that cannot be attributed to maternal intelligence and family sociodemographic variables. Follow-up of this sample will determine the predictive significance of these delays. In the meantime, routine neurodevelopmental screening of infants with isolated craniosynostosis is recommended.
Languageeng
Pub Type(s)Comparative Study
Journal Article
Research Support, N.I.H., Extramural
PubMed ID17440368
  
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