Glaucoma secondary to spherophakia/ectopia lentis and megalocornea

MONDO:0016559

Glaucoma secondary to spherophakia/ectopia lentis and megalocornea is a rare, genetic, non-syndromic developmental defect of the eye disorder characterized by congenital megalocornea associated with spherophakia and/or ectopia lentis leading to pupillary block and secondary glaucoma. Additional features may include flat irides, iridodonesis, axial myopia, very deep anterior chambers, miotic, oval pupils without well-defined borders, ocular pain and irritability manifesting as conjunctival injection, corneal edema and central scarring, as well as a high arched palate.

Also known as: megalocornea-spherophakia-secondary glaucoma syndrome

8 clinical trials for this condition and its sub-types, 0 tagged with Glaucoma secondary to spherophakia/ectopia lentis and megalocornea itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Hereditary glaucoma (50) ↑ Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma (0)

Including sub-types (8) Tagged with Glaucoma secondary to spherophakia/ectopia lentis and megalocornea (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.