Apert syndrome in a newborn infant without craniosynostosis.

Clicks: 338
ID: 43640
2012
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Abstract
Apert syndrome is a rare congenital disorder characterized by irregular craniosynostosis especially of the coronal suture. We report a case of Apert syndrome confirmed by molecular genetic analysis in a newborn infant, who did not have craniosynostosis at birth. Because this disturbance in osteogenesis may vary in timing and extent, we suggest that this diagnosis be considered even in the absence of this hallmark finding.
Reference Key
coomaralingam2012apertthe Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Coomaralingam, Sivaroopi;Roth, Philip;
Journal the journal of craniofacial surgery
Year 2012
DOI
10.1097/SCS.0b013e31824de344
URL
Keywords
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