Cerebroretinal microangiopathy with calcifications and cysts 2

MONDO:0015026

Any Coats plus syndrome in which the cause of the disease is a mutation in the STN1 gene.

Also known as: Coats plus syndrome caused by mutation in STN1, STN1 Coats plus syndrome, cerebroretinal microangiopathy with calcifications and cysts 2, cerebroretinal microangiopathy with calcifications and cysts type 2, CRMCC2

15 clinical trials for this condition and its sub-types, 0 tagged with Cerebroretinal microangiopathy with calcifications and cysts 2 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Coats plus syndrome (0)

Including sub-types (15) Tagged with Cerebroretinal microangiopathy with calcifications and cysts 2 (0)

Trials to join now! 5 Not yet recruiting 1 Not yet finished but already full! 1 Completed 7 Terminated 1

VR headsets tested as a possible treatment for blindness

Disease control Stopped early

This study tested whether using a virtual reality headset for one-hour sessions could help regenerate damaged optic nerves and improve vision in people with glaucoma or other retinal diseases. The idea came from promising results in rodents. However, the trial was terminated earl…

Sponsor: Stanford University • Aim: Disease control

Last updated Jun 27, 2026 08:03 UTC

Cerebroretinal microangiopathy with calcifications and cysts 2

Where it sits in the disease tree

VR headsets tested as a possible treatment for blindness