• A case of congenital cerulean cataract
• A case of congenital cerulean cataract
• A CRYBB2 mutation in a Taiwanese family with autosomal dominant cataract
• Analysis of disease-causing gene mutation in three Chinese families with congenital inherited cataract
• Cerulean Cataract
• Cerulean cataract
• Cerulean cataract
• Cerulean cataract
• Cerulean cataract
• Congenital cataract - clinical and morphological aspects
• Congenital cerulean cataract
• Congenital cerulean cataract
• Corneal ectasia, cerulean (blue dot) cataract with acute hydrops in a child with Down's syndrome and hypothyroidism - a rare presentation
• Familial Cataracts: Profile of Patients and Their Families at a Child Eye Care Tertiary Facility in a Developing Country
• In vivo quasi-elastic light scattering detects molecular changes in the lenses of adolescents with Down syndrome
• In-vivo anterior segment OCT imaging provides unique insight into cerulean blue-dot opacities and cataracts in Down syndrome
• Multicoloured lenticular opacities in a case of cerulean cataract
• Rare Coexistence of Bilateral Congenital Sutural and Cortical Blue Dot Cataracts
• Whole Exome Sequencing Reveals a Mutation in CRYBB2 in a Large Mexican Family with Autosomal Dominant Pulverulent Cataract