Congenital stationary night blindness 1B
MONDO:0009758Any congenital stationary night blindness in which the cause of the disease is a mutation in the GRM6 gene.
Also known as: CSNB1B, GRM6 congenital stationary night blindness, congenital stationary night blindness 1B, congenital stationary night blindness caused by mutation in GRM6, congenital stationary night blindness type 1B, night blindness, congenital stationary (complete), 1B, autosomal recessive, CSNB, complete, autosomal recessive, night blindness, congenital stationary, complete, autosomal recessive
46 clinical trials for this condition and its sub-types, 0 tagged with Congenital stationary night blindness 1B itself.
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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
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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