Clinicians often discover a retinoschisis during a peripheral retinal exam. However, the finding can occur within the posterior pole and surprise the examining provider. There are numerous etiologies of maculopathy associated with retinoschisis – also called foveoschisis. These include juvenile X-linked retinoschisis, myopic foveoschisis, optic disc pit maculopathy, autosomal recessive foveoschisis, medication induced foveoschisis, or even idiopathic classifications. The following case report will describe a patient with unilateral foveoschisis. Though visually symptomatic, the condition remained stable since 2013 and as such deferred any surgical intervention. It is important to recognize and understand the pathology, natural history, and prognosis of foveoschisis in order to monitor vision and potential complications. Regardless of the foveoschisis nature, the best diagnostic tool to monitor the condition is optical coherence tomography (OCT). Differentiating the cause will guide the examiner regarding an appropriate follow up schedule, monitoring for potential sequelae, and accurate education. CE Notification: This article is available as a COPE accredited CE course. You may take this course for 1-hour credit. Read the article and take the qualifying test to earn your credit. Click here to Enroll (https://www.crojournal.com/foveal-retinoschisis-case-report-and-clinical-review) Please check COPE course expiry date prior to enrollment. The COPE course test must be taken before the course expiry date.