Analysis of CYP1B1 Gene Mutations in Patients with Primary Congenital Glaucoma

Abstract excerpt

Abstract Primary congenital glaucoma (PCG) is the most common type of infantile glaucoma, yet it remains a relatively rare disease, because the disease is often transmitted in an autosomal recessive pattern. However, PCG occurs up to 10 times more frequently in certain ethnic and geographical groups where consanguineous relationships are common. The aim of this study was to investigate the distribution of...

Topics

Share this publication in a Topic to start or enrich a Post.

• Share to Glaucoma and retinal disorders
• Share to Retinal Diseases and Treatments
• Share to Retinopathy of Prematurity Studies