than 1% of cases [1]. While parathyroid carcinoma is often associated with several clinical manifestations and significant mortality, most patients with pHPT are asymptomatic. Symptomatic patients present with kidney and skeletal complications as well as nonspecific signs and symptoms of calcium excess [1].pHPT is a genetically heterogeneous disease with either sporadic or inherited presentation. pHPT is mostly sporadic [2][3][4][5]. In about 15% of all cases, pHPT occurs as part of an inherited disorder, most of which are caused by germline mutations of known HPT-susceptibility genes [2][3][4][5]. The most common hereditary syndromes associated with HPT are multiple endocrine neoplasia types 1 (MEN1), 2A (MEN2A), 4 (MEN4), and hyper-