Somatic mutations in GATA1, preventing the synthesis of GATA1-FL, predispose newborn Down Syndrome (DS) patients to develop (in 10–20% of cases) transient myeloproliferative disease (TMD) (Wechsler et al., 2002; Xu et al., 2003; Hitzler and Zipursky, 2005). Here, GATA1 is linked to Dravet syndrome.