Joubert syndrome 20
MONDO:0013994Any Joubert syndrome in which the cause of the disease is a mutation in the TMEM231 gene.
Also known as: JBTS20, Joubert syndrome 20, Joubert syndrome caused by mutation in TMEM231, Joubert syndrome type 20, TMEM231 Joubert syndrome
17 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
-
Robots as rehab coaches: a new approach to retraining coordination in ataxia
Disease control OngoingThis trial tests whether robot-assisted neurorehabilitation can improve coordination, balance, and walking in adults with ataxia, a condition that affects movement control. Participants will receive either robotic or standard rehabilitation, and researchers will measure changes i…
Phase: NA • Sponsor: Somogy Megyei Kaposi Mór Teaching Hospital • Aim: Disease control
Last updated Jul 31, 2026 00:00 UTC
-
Can a gentle brain zap help people with ataxia walk better?
Symptom relief OngoingThis study tests whether a non-invasive brain stimulation technique called transcranial direct current stimulation (tDCS) can improve movement in people with degenerative ataxia, a rare condition that damages the cerebellum and impairs balance and coordination. Sixteen participan…
Phase: NA • Sponsor: University of Cagliari • Aim: Symptom relief
Last updated Jun 27, 2026 08:00 UTC