Saethre-Chotzen syndrome

MONDO:0007042

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, 3 tagged with Saethre-Chotzen syndrome itself.

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Where it sits in the disease tree

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↑ Acrocephalosyndactyly (13)

Including sub-types (4) Tagged with Saethre-Chotzen syndrome (3)

Trials to join now! 1 Not yet finished but already full! 1 Completed 1 Terminated 1

Nano-ink gel could replace repeated skull surgeries for kids with rare genetic disorders

Disease control Recruiting now

This early-stage study aims to develop a personalized treatment for children with syndromic craniosynostosis, a group of rare genetic disorders where skull bones fuse too early. The approach uses a nano-engineered gel to deliver custom genetic medicine directly to the affected ar…

Sponsor: Fondazione Policlinico Universitario Agostino Gemelli IRCCS • Aim: Disease control

Last updated Sep 10, 2026 00:00 UTC

Saethre-Chotzen syndrome

Where it sits in the disease tree

Nano-ink gel could replace repeated skull surgeries for kids with rare genetic disorders