Olufemi E Adams, Olufunmilola Adeleye, Musse Hussein, Ameay Naravane, Tyler Looysen, Michael A Simmons, Peter H Tang, Sandra R Montezuma
PURPOSE: To describe the syndromic, clinical, and retinal findings of a patient with an extremely-rare genetic condition known as Hardikar Syndrome (HS) with presentation of optical coherence tomography (OCT), fundus autofluorescence (FAF), fluorescein angiographic (FA), and indocyanine green angiographic (ICG) findings. METHODS: Clinical course was detailed and followed over time with examinations and multimodal imaging. PATIENT AND RESULTS: A 17-year-old patient with HS was referred for possible retinitis pigmentosa...
August 15, 2023: Retinal Cases & Brief Reports