Searchable abstracts of presentations at key conferences in endocrinology

ea0099ep8 | Calcium and Bone | ECE2024

Novel germline variant of CDC73 identified during screening for familial primary hyperparathyroidism

Muntean Andreea , Mazarico Altisent Isabel , Capel Flores Ismael , Casamitjana Espuna Laia , Hernandez Lazaro Alba , Barcons Vilaplana Santiago , Guirao Garriga Xavier , Baena Diez Neus , Romero Gregori Ana , Bella Burgos Berta , Arsentales Montalva Valeria , Jover Gornall Judith , Rigla Cros Mercedes

Background: Hyperparathyroidism jaw-tumor syndrome (HPT-JT) is a rare and underdiagnosed cause of familial primary hyperparathyroidism (incidence <1/1000000). It is caused by a pathogenic variant in the CDC73 (or HRPT2) gene that encodes parafibromin. Patients with HPT-JT have a 15–20% risk of developing parathyroid carcinoma. Other related conditions are jaw tumors in 30% of cases, kidney abnormalities in 15% of cases, and uterine tumors in 50% of c...