GUCY2D-related recessive retinopathy
MONDO:0100453A retinopathy caused by biallelic variants in the GUCY2D gene.
Also known as: recessive GUCY2D retinopathy, CORD6, CRB, GUCY2D Leber congenital amaurosis, GUCY2D cone-rod dystrophy, LCA, LCA1, Leber congenital amaurosis 1
26 clinical trials for this condition and its sub-types, 0 tagged with GUCY2D-related recessive retinopathy itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of GUCY2D-related recessive retinopathy
-
Leber congenital amaurosis 1 1 trial
-
VR headsets tested as a possible treatment for blindness
Disease control Stopped earlyThis 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
-
Scientists dig into DNA to unravel rare eye disorders
Knowledge-focused Stopped earlyThis study looked at over 100 people with inherited retinal dystrophies, a group of rare eye diseases that can cause vision loss. Researchers collected genetic and eye exam data to find links between specific gene mutations and symptoms. The goal was to better understand these di…
Sponsor: Fondation Ophtalmologique Adolphe de Rothschild • Aim: Knowledge-focused
Last updated Jun 27, 2026 08:03 UTC