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Br J Ophthalmol 87:302-304 doi:10.1136/bjo.87.3.302
  • Original Article
    • Clinical science

Phenotype of cytochrome P4501B1 gene (CYP1B1) mutations in Japanese patients with primary congenital glaucoma

Table 3

Anterior segment appearance in primary congenital glaucoma with or without CYP1B1 mutations

Corneal opacity Ruptures in Descemet‘s membrane High insertion of iris
Mutation group 20/21 eyes (95.2%) 8/21 eyes (38.1%) 17/21 eyes (80.9%)
No mutation group 35/38 eyes (92.1%) 16/38 eyes (42.1%) 32/38 eyes (84.2%)

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