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Glaucoma 3A

MONDO:0009277

An autosomal recessive form of congenital glaucoma caused by mutation(s) in the CYP1B1 gene, encoding cytochrome P450 1B1.

Also known as: buphthalmos, Primary Congenital glaucoma 3A, glaucoma 3, primary congenital, type a, glaucoma 3A, primary open angle, congenital, juvenile, or adult onset, GLC3A, glaucoma 3, primary congenital, A, glaucoma, congenital, glaucoma, primary open angle, adult-onset

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

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Broader categories

Disease (680) Glaucoma (196) Hereditary disease (176) Eye disorder (102) Human disease (14) Congenital glaucoma (6) Disorder of orbital region (3) Disease of genetic or genomic mechanism (2) Primary congenital glaucoma (2) Disorder of visual system (1)
Trials to join now! 1 Not yet recruiting 1 Not yet finished but already full! 1 Completed 2 Terminated 1
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  • Glaucoma patients: could this supplement save your sight?

    Disease control Recruiting now

    This study tests whether a daily supplement called BrudyGlauco (containing DHA and citicoline) can help protect eyesight in people with glaucoma. About 108 participants will take either the supplement or a placebo for 12 months. The goal is to see if it slows vision loss and impr…

    Phase: NA • Sponsor: Institut Catala de Retina • Aim: Disease control

    Last updated Jun 27, 2026 08:11 UTC

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