Akella Madhuri

Neonatal-Onset Congenital Ectropion Uveae May Be Caused by a Distinct CYP1B1 Pathologic Variant.

NO-CEU appears to be a phenotypic marker for specific CYP1B1 genotypes, one of which is [c.1169G>A(p.Arg390His)] in our study population. Phenotype recognition is helpful to characterize the underlying genetic variants.

Phacomorphic Glaucoma.

Weill-Marchesani Syndrome with Secondary Angle Closure Glaucoma.

Pigment Dispersion Syndrome.