Jackson-Weiss syndrome

MONDO:0007400

Jackson-Weiss syndrome (JWS) is a rare genetic disorder characterized by foot malformations (tarsal and metatarsal fusions; short, broad, medially deviated great toes) and in some patients craniosynostosis with facial anomalies. Hands are normal in affected patients.

Also known as: JWS, Jackson-Weiss syndrome, craniosynostosis-midfacial hypoplasia-foot abnormalities syndrome, craniosynostosis, midfacial hypoplasia, and foot abnormalities

2 clinical trials for this condition and its sub-types, 0 tagged with Jackson-Weiss syndrome itself.

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Where it sits in the disease tree

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Part of

↑ Acrocephalosyndactyly (13)

Including sub-types (2) Tagged with Jackson-Weiss syndrome (0)

Trials to join now! 1 Completed 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

Jackson-Weiss syndrome

Where it sits in the disease tree

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