“…The diagnosis of iridoschisis was made based on the clinical appearance, age of onset, laterality and whether the condition is progressive or with co-existent ACG. Similar to this, studies have revealed that the sixth to seventh decades of life are when iridoschisis typically manifests (Pieklarz et al, 2020;Schmitt, 1922;Loewenstein & Foster, 1945;Seth et al, 2018;Chen et al, 2017;Gogaki, Tsolaki, Tiganita, Skatharoudi, & Balatsoukas, 2011) although Pegu, Jain, and Dubey (2020) observed that the average age of presentation was 49 years or the fifth decade (Pegu et al, 2020).…”