“…29 A point mutation in the RET proto-oncogene in exons 10,11,13,14,15, and 16 (codon 918) has been observed in MEN 2 syndrome. 7,30 In MEN 2B, clinical evidence of MTC usually becomes apparent in adolescence but has also been reported in childhood. 31 Mucosal neuromas occur at an early age, typically before the presentation of MTC and phaeochromocytoma.…”