Cure My Disease

Don't miss your cure!

Home News Browse Soon ready About
Log in / Sign up

Arthrogryposis

MONDO:0008779

A rare, non-progressive congenital disorder characterized by multiple joint contractures which are present at birth.

Also known as: Arthrogryposes, congenital multiple, congenital multiple Arthrogryposes, congenital multiple arthrogryposis

18 clinical trials for this condition and its sub-types, 4 tagged with Arthrogryposis itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Hereditary neurological disease (5791) ↑ Movement disorder (805)

Sub-types of Arthrogryposis

  • Freeman-Sheldon syndrome 1 trial
    1 sub-type
    • Whistling face syndrome, recessive form 0 trials
  • Congenital contractural arachnodactyly 1 trial
  • Boylan dew greco syndrome 0 trials
  • Distal arthrogryposis Moore weaver type 0 trials
  • Massa casaer ceulemans syndrome 0 trials
Including sub-types (18) Tagged with Arthrogryposis (4)
Trials to join now! 1 Not yet recruiting 2 Not yet finished but already full! 1
Sort by
  • Running reimagined: could an adapted program get kids moving?

    Symptom relief By invitation only

    This study tests a 6-8 week running program adapted for children with mobility challenges like cerebral palsy. The program uses a special device called a RaceRunner to help kids participate. Researchers will measure endurance, speed, and heart rate to see if the program improves …

    Sponsor: Northwestern University • Aim: Symptom relief

    Last updated Aug 20, 2026 00:00 UTC

Cure My Disease

Helping patients find clinical trials that match their disease.

Why was Cure my disease built?

Explore

Home News Browse Glossary About Terms of use Contact us

This is a site from Cyber and Space