A Rare Case Series on Axenfeld - Rieger Syndrome in Mother and Daughter without Glaucoma

Shilpa Vasanth

Abstract: Description of clinical findings of a rare case of axenfeld reiger syndrome spotted ina mother and daughter, with normal IOP. Rare autosomal dominant pattern Axenfeld Reiger syndrome seen in a 31 year old mother - Both eyes having microcornea, normal intraocular pressure with Right eye cornealopacity, iridogoniodysgenesis with polymegathism and pleomorphism on specular microscopy and left eye iridogoniodysgenesis with Dshapedpupil, dental findings showing hypoplastic maxilla and malocclusion which was dentally rehabilitated.8 year old daughter has both eyes normal IOP, right eye posterior embryotoxon and correctopia and left eye posterior embrotoxon, atrophic iris andcorrectopia with dental findings of malocclusion and hypoplastic maxilla.

Keywords: iridogoniodysgenesis, axenfeld reiger syndrome, Glaucoma, Glaucoma syndromes, iris abnormalities