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Article

Meta-analysis of CYP1B1 gene mutations in primary congenital glaucoma patients.

European journal of ophthalmology - 1 Nov 2021

Haddad Amine, Ait Boujmia Oum Kaltoum, El Maaloum Loubna, Dehbi Hind

Abstract excerpt

Primary congenital glaucoma (PCG) is a rare and severe form of glaucoma and is usually transmitted as an autosomal-recessive disease. However, PCG is more common in certain ethnic and geographic groups where consanguineous relationships are common. The importance of this review is to inspect the mutations in the cytochrome P450 1B1 gene (CYP1B1) and to highlight the interest of the genetic study of CYP1B1...

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Corneal surgery and disorders
Cytochrome P-450 CYP1B1
DNA Mutational Analysis
Glaucoma
Glaucoma and retinal disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Retinopathy of Prematurity Studies

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PMID: 34020567
DOI: 10.1177/11206721211016308

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