Frank-ter Haar syndrome associated with sagittal craniosynostosis and raised intracranial pressure

<p>Abstract</p> <p>Background</p> <p>Frank-ter Haar syndrome is a rare disorder associated with skeletal, cardiac, ocular and craniofacial features including hypertelorism and brachycephaly. The most common underlying genetic defect in Frank-ter Haar syndrome appears to...

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Bibliographic Details
Main Authors: Bendon Charlotte L, Fenwick Aimée L, Hurst Jane A, Nürnberg Gudrun, Nürnberg Peter, Wall Steven A, Wilkie Andrew OM, Johnson David
Format: Article
Language:English
Published: BMC 2012-11-01
Series:BMC Medical Genetics
Subjects:
Online Access:http://www.biomedcentral.com/1471-2350/13/104