Abstract
Gardner Syndrome is a phenotypic variant of Familial Adenomatous Polyposis (FAP) characterized by extracolonic manifestations including pigmented ocular fundus lesions with malignant polyps in the large intestine. We present the case of a 41-year-old female with FAP, who presented with numerous congenital hypertrophy of the retinal pigment epithelium ocular lesions. We describe the case report along with a literature review of ocular findings in Gardner syndrome.
Keywords
Gardner Syndrome, Familiar Adenomatous Polyposis, Eye, Syndrome