Abstract
This study is linked to the ongoing Thematic Project (2021/02752-6), directly contributing to Subproject 5 of this Thematic Project. Multiple Endocrine Neoplasia type 2 (MEN2) is an autosomal dominant genetic syndrome characterized by associations of endocrine-origin tumors and classified into subtypes MEN2A and MEN2B based on clinical manifestations. The most important and predominant cl…