Congenital stationary night blindness 2A
MONDO:0010241Any congenital stationary night blindness in which the cause of the disease is a mutation in the CACNA1F gene.
Also known as: CACNA1F congenital stationary night blindness, CSNB, incomplete, X-linked, congenital stationary night blindness caused by mutation in CACNA1F, congenital stationary night blindness type 2A, night blindness, congenital stationary (incomplete), 2A, X-linked, CSNB2A, night blindness, congenital stationary, type 2, night blindness, congenital stationary, type 2A
46 clinical trials for this condition and its sub-types, 0 tagged with Congenital stationary night blindness 2A 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