Rett Syndrome (RTT) is a disorder caused by mutations in Methyl CpG binding protein 2 (MECP2), Forkhead box G1 (FOXG1) or Cyclin-dependent kinase-like 5 (CDKL5) genes [1–3] Although the phenotype of patients with mutations in MECP2 differs from the phenotype of patients with FOXG1 or CDKL5 mutations, there are some similarities in the clinical profile that overlap with RTT. The gene discussed is FOXG1; the disease is Rett syndrome.