A two-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family: clinical presentations, pathological characteristics and genetic analysis: a case report

• Hlavní autoři: Dun Yang (Autor), Jiaoyun Zheng (Autor), Fei Tang (Autor), Qiongzhi He (Autor), Hui Huang (Autor), Peng Zhou (Autor)
• Médium: Kniha
• Vydáno: BMC, 2022-09-01T00:00:00Z.
• Témata: article
• On-line přístup: Connect to this object online.

Abstract Background Hyperparathyroidism-Jaw Tumor (HPT-JT) is caused by inactivating germline mutations of CDC73. This hereditary disease can present with a range of symptoms. Jaw ossifying fibroma (OF) is one of the most important clinical presentations, affecting 30% of HPT-JT patients. However, O...