Although both hypertrophic cardiomyopathy and chylothorax are common in Noonan's syndrome [4], no variants have been identified in the genes related to Noonan syndrome (PTPN11, SOS1, RAF1, RIT1, KRAS, NRAS, SHOC2, CBL, BRAF, SOS2, MRAS, RRAS, LZTR1, RRAS2, HRAS, MAP2K1, MAP2K2, and PPP1CB) by a targeted next-generation sequencing panel testing. The gene discussed is HRAS; the disease is Noonan syndrome.