hrp0098rfc10.4 | Multisystem Endocrine Disorders | ESPE2024
Blinstein Marc
, Fradkin Mark
, Rutkauskiene Giedre
, Navardauskaite Ruta
Introduction: PTEN hamartoma tumor syndrome (PTHS), a rare genetic disorder, increases the risk of endocrine-related benign and malignant tumors like thyroid, endometrial, breast, and kidney tumors, as well as syndromes like Cowden syndrome (CS), which can cause genodermatosis. The MUTYH gene increases colon cancer risk. Pathogenic MUTYH and PTEN gene variants are autosomal dominantly inherited and 50% likely to pass on.<p class=...