Choroidal dystrophy, central areolar 2
MONDO:0013137Any central areolar choroidal dystrophy in which the cause of the disease is a mutation in the PRPH2 gene.
Also known as: PRPH2 central areolar choroidal dystrophy, central areolar choroidal dystrophy caused by mutation in PRPH2, choroidal dystrophy, central areolar 2, choroidal dystrophy, central areolar type 2, CACD2, macular dystrophy, progressive
25 clinical trials for this condition and its sub-types, 0 tagged with Choroidal dystrophy, central areolar 2 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