Pelviscapular dysplasia

MONDO:0009845

Pelviscapular dysplasia (Cousin syndrome) is characterized by the association of pelviscapular dysplasia with epiphyseal abnormalities, congenital dwarfism and facial dysmorphism.

Also known as: Cousin syndrome, familial pelvis-scapular dysplasia, pelviscapular dysplasia, COUSIN syndrome, craniofacial Dysmorphism, hypoplasia of scapula and pelvis, and short stature, craniofacial dysmorphism, hypoplasia of scapula and pelvis and short stature

1 clinical trial for this condition and its sub-types, 0 tagged with Pelviscapular dysplasia itself.

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Where it sits in the disease tree

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Part of

↑ Dysostosis (85) ↑ Congenital limb malformation (61) ↑ Non-syndromic limb reduction defect (35)

Including sub-types (1) Tagged with Pelviscapular dysplasia (0)

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

Pelviscapular dysplasia

Where it sits in the disease tree

Kids test new bionic foot design