Loading

Case Report Open Access
Volume 3 | Issue 1 | DOI: https://doi.org/10.46439/ophthalmology.3.023

Ocular Manifestation of Familial Adenomatous Polyposis

  • 1Institute of Ophthalmology and Visual Sciences Rutgers New Jersey Medical School, Newark, NJ, USA
  • 2Rutgers Robert Wood Johnson Medical School, Piscataway, NJ, USA
+ Affiliations - Affiliations

Corresponding Author

Neelakshi Bhagat, bhagatne@njms.rutgers.edu

Received Date: April 22, 2021

Accepted Date: April 06, 2021

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

Author Information X