Saethre-Chotzen syndrome

Saethre-Chotzen syndrome (SCS) is an inherited craniosynostosis syndrome characterized by unilateral or bilateral coronal synostosis, facial asymmetry, ptosis, strabismus and small ears with prominent crus, among other less common manifestations.

Also known as: ACS3, SCS, Saethre Chotzen Syndrome, Saethre-Chotzen syndrome, Saethre-Chotzen syndrome with or without eyelid anomalies, acrocephalosyndactyly type 3, type III Acrocephalosyndactyly, ACS 3

4 clinical trials for this condition and its sub-types.