Case Report

The Unforeseen Diagnosis: Hyperparathyroidism-Jaw Tumour Syndrome Case Report and Review of the Literature

Table 2

Genetic mutations assessed.

Genetic mutation

MEN1
CDC73
CDKN1A
CDKN1B
RET
AP2S1
CASR
GCM2

MEN1: multiple endocrine neoplasia 1; CDC73: cell division cycle 73; CDKN1A: cyclin-dependent kinase inhibitor 1A; CDKN1B: cyclin-dependent kinase inhibitor 1B; RET: rearranged during transfection; AP2S1: adaptor-related protein complex 2 subunit sigma 1; CASR: calcium sensing receptor; GCM2: glial cells missing transcription factor 2.