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Maroteaux Fonfria syndrome

MONDO:0023699

Also known as: apert syndrome with polydactyly of hands and feet, apparent apert syndrome with polydactyly

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

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Where it sits in the disease tree

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Part of

↑ Apert syndrome (11)

Including sub-types (2) Tagged with Maroteaux Fonfria 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