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CYP1B1-related glaucoma with or without anterior segment dysgenesis

MONDO:0800472

Any primary congenital glaucoma in which the cause of the disease is a mutation in the CYP1B1 gene.

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

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Sub-types

Anterior segment dysgenesis 6 (1) Glaucoma 3A (1)

Broader categories

Disease (618) Glaucoma (177) Hereditary disease (172) Eye disorder (97) Human disease (14) Congenital glaucoma (5) Disorder of orbital region (3) Disease of genetic or genomic mechanism (2) Disorder of visual system (1) Primary congenital glaucoma (1)

Trials to join now! 9 Not yet finished but already full! 2 Completed 1 Terminated 2

App aims to clear up glaucoma drop confusion

Knowledge-focused Completed

This study tested whether a simple app, available in English, Spanish, and Cantonese, could help glaucoma patients better remember their multiple eye drop schedules. Twenty participants either used the app or received standard instructions. After one month, researchers compared h…

Phase: NA • Sponsor: University of California, San Francisco • Aim: Knowledge-focused

Last updated Jun 27, 2026 08:07 UTC