RIT1 and Noonan syndrome: Including the patient in this report, this mutation has been reported in 18% (25/141) of patients with RIT1‐associated Noonan syndrome (Aoki et al., 2013; Bertola et al., 2014; Cave et al., 2016; Cizmarova et al., 2016; Koenighofer et al., 2016; Kouz et al., 2016; Yaoita et al., 2016).