1989; Wallace et al. 2014; Bohnsack 2016; Mauri et al. 2016; Laroche & Nkrumah 2020). The paper by Wallace et al. (2014) described three patients (from two families) with OI type I and primary open‐angle glaucoma (POAG). Central corneal thickness (CCT) measurements were lower in the affected patients compared to healthy controls. Genetic testing of MYOC, a known glaucoma‐associated gene, was performed but no mutations were found in any of the patients. Laroche & Nkrumah (2020) reported on a 57‐year‐old woman with POAG. The gene discussed is MYOC; the disease is glaucoma.