Year: 2024
Type: article
Study design: Case Report
Abstract: Persistent hyperplastic primary vitreous (PHPV) is a rare congenital ophthalmic developmental disorder that occurs as a result of incomplete regression of the embryonic hyaloid vasculature. Usually, it presents unilaterally but it can also present bilaterally which is rare. It conventionally manifests with leukocoria, microphthalmia and retinal dysplasia which has a poor visual prognosis. Nevertheless, there is a paucity of awareness on instances of PHPV in teenage without typical manifestations. This article dispenses the presentation of an atypical PHPV and reviews the contemporary comprehension for this diagnosis. It describes a 12-year-old boy with bilateral PHPV who came for routine ophthalmic examination with no significant history which discriminates this presentation from typical PHPV. It is imperative to raise perception of congenital ocular diseases and the significance of dilated fundoscopy and provide timely management.
Authors: Ishwarya Rajaprabhu, Shruthi Devi Suresh, Premnath Gnaneswaran, Abijith Vasan Kumaran
Institution: Chettinad Academy of Research and Education
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: diamond
OpenAlex ID: W4405913681