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Familial clubfoot due to PITX1 point mutation

MONDO:0017383

Also known as: hereditary clubfoot due to PITX1 point mutation

1 clinical trial 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) Clubfoot (18) Human disease (14) Developmental defect during embryogenesis (8) Skeletal system disorder (4) Congenital limb malformation (3) Disease of genetic or genomic mechanism (2)

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