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#4149 A case of multiple endocrine neoplasia type 1 (MEN1) phenotype caused by CDC73 mutation

Introduction: CDC73 gene, also known as HRPT2 gene, its related diseases (CDC73-Related Disorders) mainly include hyperparathyroidism-jaw tumor syndrome (HPT-JT), parathyroid adenocarcinoma, familial isolated hyperparathyroidism (FIHP), which is autosomal dominant inheritance.

Conference:

Presenting Author: Tan H

Authors: Tan H, Chi Y,

Keywords: CDC73, HPT-JT, PNET, phenotype,