HSPA9 and even-plus syndrome: According to the 2015 guidelines of the American College of Medical Genetics and Genomics, HSPA9 c.882_c.883delAG and c.613A > G were pathogenic and likely pathogenic variants, respectively, with c.882_c.883delAG being a reported variant identified in patients with EVEN‐plus syndrome (Royer‐Bertrand et al., 2015).