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

More general terms

• genetic syndrome (multisystem disorder)

Database

• OMIM: https://mirror.omim.org/entry/180750