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Frank-ter Haar syndrome associated with sagittal craniosynostosis and raised intracranial pressure
BACKGROUND: 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 be a mutation in the SH3PXD2B gene on chromosome 5q35....
Main Authors: | , , , , , , , |
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Format: | Online Article Text |
Language: | English |
Published: |
BioMed Central
2012
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Subjects: | |
Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3532175/ https://www.ncbi.nlm.nih.gov/pubmed/23140272 http://dx.doi.org/10.1186/1471-2350-13-104 |