In 2007, Menten et al. [9] reported SRS patients with the microdeletion of the 12q14.3 region encompassing different genes including HMGA2 and LEMD3 (an OMIM Disease Causing gene associated with Buschke-Ollendorff syndrome and Osteopoikilosis with or without melorheostosis). Here, HMGA2 is linked to Silver-Russell syndrome.