Multiple Endocrine Neoplasia Type 2 (MEN-2): An Update. Multiple endocrine neoplasia type 2 (MEN-2) is an autosomal dominant hereditary cancer syndrome. The disorder is caused by missense mutations of the RET proto-oncogene that result in their gain of function. Three distinct clinical subtypes of MEN-2 are characterized: MEN-2A, MEN-2B, and familial MTC (FMTC). The precise RET mutations may su...

Introduction Antipsychotics have shown their interest in several pathologies of the child and adolescent. However, this vulnerable population, they are not without adverse effects. Depending on type molecule used, classical neuroleptics or second generation antipsychotics, but also within these own classes, profile tolerance effects differs. In sense, children treated with psychotropic drugs a ...