Leber congenital amaurosis 14
MONDO:0013231Any Leber congenital amaurosis in which the cause of the disease is a mutation in the LRAT gene.
Also known as: LCA14, LRAT Leber congenital amaurosis, Leber congenital amaurosis 14, Leber congenital amaurosis caused by mutation in LRAT, Leber congenital amaurosis type 14, retinal dystrophy, early-onset severe, retinal dystrophy, early-onset Severe, LRAT-related, retinitis pigmentosa, juvenile
33 clinical trials for this condition and its sub-types.
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VR headsets tested as a possible treatment for blindness
Disease control TerminatedThis 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…
Phase: NA • 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 TerminatedThis 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