ea0090p663 | Endocrine-related Cancer | ECE2023
Butz Henriett
, Nagy Petra
, Papp Janos
, Bozsik Aniko
, Grolmusz Vince
, Pocza Timea
, Patocs Attila
Hereditary genetic variants are common among patients with endocrine tumours. Some specific clinical conditions are informative for certain monogenic syndromes (i.e., Carney complex, MEN1, MEN2, von Hippel Lindau syndrome) but manifestations characteristic for these syndromes occur more commonly as apparently sporadic. Other tumours, i.e., pheochromocytoma/paragangliomas (PPGL) are linked to multiple genes, hence a multigene approach in molecular genetic testing strategy is re...