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Apert syndrome

MONDO:0007041

Apert syndrome (AS) is a frequent form of acrocephalosyndactyly, a group of inherited congenital malformation disorders, characterized by craniosynostosis, midface hypoplasia, and finger and toe anomalies and/or syndactyly.

Also known as: ACS1, Apert syndrome, acrocephalosyndactyly type 1, acrocephalosyndactyly type I, type I Acrocephalosyndactyly, ACS 1, ACS 2, Apert-Crouzon disease

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

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Sub-types

Maroteaux Fonfria syndrome (0)

Broader categories

Disease (680) Musculoskeletal system disorder (207) Hereditary disease (176) Bone disorder (51) Syndromic disease (25) Craniosynostosis (15) Human disease (14) Developmental defect during embryogenesis (8) Skeletal system disorder (4) Congenital limb malformation (3)

Trials to join now! 3 Not yet recruiting 1 Not yet finished but already full! 2 Completed 3 Terminated 3

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

Disease control Not yet recruiting

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 Jun 27, 2026 12:09 UTC