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#1329 The MEN2B Due to de Novo Mutation M918T at Algiers

Introduction: The MEN2B, or Gorlin syndrome is a very rare disorder where there are a medullary cancer of thyroide associated with pheochromocytoma and other clinical signs such as a ganglion – neuromatose or a Marfan syndrome. The MEN2B belongs MEN2 are rare hereditary disease, transmitted as an autosomal dominant mutations linked to the RET proto-oncogene.

Conference: 13th Annual ENETSConcerence (2016)

Presenting Author:

Authors: Chikouche A,

Keywords: MEN2B, de novo mutation, genotypic analysis,