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Robinow-Sorauf syndrome; craniosynostosis-bifid hallux syndrome
Genetics:
- autosomal dominant
- associated with defects in TWIST1
Clinical manifestations:
- minor skull & limb anomalies
- very similar to Saethre-chotzen syndrome
General
genetic syndrome (multisystem disorder)
Database Correlations
OMIM 180750
References
OMIM :accession 180750