PIEZO1 and dehydrated hereditary stomatocytosis: Mutations in both human PIEZO1 and human PIEZO2 have been identified among patients suffering from channelopathy diseases, such as dehydrated hereditary stomatocytosis (DHSt), generalized lymphatic dysplasia (GLD), and distal arthrogryposis type 5 (DA5), in which osmoregulation is disturbed (Albuisson et al., 2013; Andolfo et al., 2013; Bae et al., 2013; Coste et al., 2013; Li et al., 2018; Lukacs et al., 2015; McMillin et al., 2014; Zarychanski et al., 2012).