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Stickler syndrome, type 5

MONDO:0013666

Any autosomal recessive Stickler syndrome in which the cause of the disease is a mutation in the COL9A2 gene.

Also known as: COL9A2 autosomal recessive Stickler syndrome, autosomal recessive Stickler syndrome caused by mutation in COL9A2, STICKLER syndrome, type V, STL5

13 clinical trials for this condition and its sub-types.

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Broader categories

Disease (680) Nervous system disorder (231) Musculoskeletal system disorder (207) Hereditary disease (176) Eye disorder (102) Retinal disorder (85) Bone disorder (51) Syndromic disease (25) Human disease (14) Osteochondrodysplasia (12)
Trials to join now! 6 Not yet recruiting 1 Completed 5 Terminated 1
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  • VR headsets tested as a possible treatment for blindness

    Disease control Terminated

    This 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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