Congenital Cataract Latest Advances
Find the Latest Research About Congenital Cataract
Last Updated: 06/30/2026
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Found 3842 publications
Erratum in: A Novel CRYBB2 Splicing Mutation Is Associated With Lens Extracellular Matrix Remodeling and Vascular Alterations in Congenital Cataract.
Journal: Investigative ophthalmology & visual science
Published: June 16, 2026
A nationwide overview of the clinical and genetic landscape of inherited eye disorders in Denmark.
Journal: Ophthalmic genetics
Published: June 11, 2026
Aqueous Humor Cytokine Profiles in Congenital Cataracts With Posterior Polar Abnormality and Associations With Postoperative Complications.
Journal: Investigative ophthalmology & visual science
Published: May 14, 2026
Can the diagnostic accuracy of newborn eye screening for congenital cataract be improved with digital imaging? The Digital Imaging versus Ophthalmoscopy (DIvO) study.
Journal: NIHR open research
Published: May 13, 2026
Congenital brain malformations associated with COL4A1 gene mutations: A case series.
Journal: Archivos argentinos de pediatria
Published: May 12, 2026
Cat Eye Syndrome in a Sudanese Infant: Congenital Cataract in the Absence of Iris Coloboma: A Case Report.
Journal: Clinical case reports
Published: May 12, 2026
Strengthening the prevention and control of visual impairment among children in China
Journal: [Zhonghua yan ke za zhi] Chinese journal of ophthalmology
Published: May 08, 2026
Longitudinal Changes in Nystagmus Following Late Treatment for Congenital Blindness.
Journal: Investigative ophthalmology & visual science
Published: May 04, 2026
Characteristics and features of ocular diseases in children born from consanguineous marriages
Journal: Vestnik oftalmologii
Published: April 28, 2026
A Novel CRYBB2 Splicing Mutation Is Associated With Lens Extracellular Matrix Remodeling and Vascular Alterations in Congenital Cataract.
Journal: Investigative ophthalmology & visual science
Published: April 16, 2026
A Rare Case of Multi-System Involvement and Hereditary Pulmonary Hypertension Caused by De Novo Heterozygous CAV1 Mutation in a Pediatric Patient.
Journal: Children (Basel, Switzerland)
Published: April 13, 2026
Last Updated: 06/30/2026