Pigment dispersion syndrome (PDS) is an autosomal dominant disorder characterized by disruption of the iris pigment epithelium (IPE) and deposition of pigment. Many patients with pigment dispersion glaucoma remain undetected, while those patients with glaucoma are. Send this article to a friend by filling out the fields below: Your name: Your friend's name: Your friend's email: Close Send Send this article to a friend by filling out the fields below: Your name: Your friend s name: Your friend s email: Close Send Patients with pigmentary glaucoma (PG) are usually asymptomatic. Pigment dispersion syndrome (PDS) is an autosomal dominant disorder characterized by disruption of the iris pigment epithelium (IPE) and deposition of. Ophthalmologist Carolina Valdivia, MD explains causes, risk factors, and treatment options for pigmentary glaucoma, a special form of open-angle glaucoma. The Pigment Dispersion Syndrome (PDS) and the Pigmentary Glaucoma (PG) are characterized by loss of pigment from the posterior surface of the iris in the mid-periphery and. Generally, glaucoma is a group of conditions all characterized by. NEI: congenital glaucoma, pigmentary glaucoma, neovascular glaucoma. PIGMENTARY GLAUCOMA Pigmentary glaucoma is a type of inherited open-angle glaucoma which develops more frequently in men than in women. Patients with pigmentary glaucoma (PG) are usually asymptomatic.



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