Antley-Bixler syndrome
MONDO:0008803Antley-Bixler syndrome is a very rare disorder characterized by craniosynostosis with midface hypoplasia, radiohumeral synostosis, femoral bowing and joint contractures.
Also known as: Antley Bixler syndrome, multisynostotic osteodysgenesis with long bone fractures, osteodysgenesis, multisynostotic with fractures, osteodysgenesis, multisynostotic, with fractures, trapezoidocephaly synostosis syndrome
3 clinical trials for this condition and its sub-types, 2 tagged with Antley-Bixler syndrome itself.
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Sub-types of Antley-Bixler syndrome
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Nano-ink gel could replace repeated skull surgeries for kids with rare genetic disorders
Disease control Recruiting nowThis 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
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New study aims to unlock secrets of rare cholesterol diseases
Knowledge-focused Recruiting nowThis natural history study is observing up to 250 people with Smith-Lemli-Opitz syndrome and related cholesterol disorders, as well as their relatives. Researchers will track symptoms, development, and lab results over several years to find better ways to measure disease progress…
Sponsor: Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) • Aim: Knowledge-focused
Last updated Aug 19, 2026 00:00 UTC