A Pilot Study on Human CYP1B1 Gene Mutations in Three Cases with Primary Congenital Glaucoma in Calabar: Benefits for Disease Management (original) (raw)

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2018, Journal of Advances in Medicine and Medical Research

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10 pages

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Background: Primary congenital glaucoma (PCG) is an inherited ocular congenital anomaly of the trabecular meshwork and anterior chamber angle, which results in optic nerve damage due to increase intraocular pressure if not properly managed. We explore CYPIBI gene mutations in three Original Research Article