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...
Main Authors: | , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2012-11-01
|
Series: | BMC Medical Genetics |
Subjects: | |
Online Access: | http://www.biomedcentral.com/1471-2350/13/104 |