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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.

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Broader categories

Disease (680) Musculoskeletal system disorder (207) Hereditary disease (176) Bone disorder (51) Syndromic disease (25) Craniosynostosis (15) Human disease (14) Apert syndrome (11) Developmental defect during embryogenesis (8) Skeletal system disorder (4)

Not yet recruiting 1 Completed 1

Kids test new bionic foot design

Knowledge-focused Completed

This study tested a new prosthetic foot for children with leg amputations or birth defects. Thirteen kids walked with the device and gave feedback on stiffness and performance. The goal was to gather ideas to improve future foot designs.

Sponsor: Össur Iceland ehf • Aim: Knowledge-focused

Last updated Jun 27, 2026 14:00 UTC