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Chromosome 16p13.3 deletion syndrome

MONDO:0022752

Also known as: RSTS, Severe, Rubinstein-Taybi syndrome, Severe

1 clinical trial for this condition and its sub-types.

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Sub-types

Rubinstein-Taybi syndrome due to 16p13.3 microdeletion (0)

Broader categories

Disease (680) Nervous system disorder (231) Musculoskeletal system disorder (207) Hereditary disease (176) Neurodevelopmental disorder (147) Intellectual disability (133) Bone disorder (51) Syndromic disease (25) Human disease (14) Chromosomal disorder (12)

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