18F-FDG PET/CT in the Hyperparathyroidism-Jaw-Tumor Syndrome.
Sign Up to like & getrecommendations! Published in 2021 at "Clinical nuclear medicine"
DOI: 10.1097/rlu.0000000000003625
Abstract: ABSTRACT Hyperparathyroidism-jaw-tumor syndrome (HPT-JTS) is a rare autosomal dominant disorder. A typical manifestation of HPT-JTS is the association of jaw-ossifying fibroma with primary hyperparathyroidism. Due to its rarity and diversity in its manifestations, it is… read more here.
Keywords: jaw tumor; fdg pet; hyperparathyroidism jaw; hyperparathyroidism ... See more keywords
Multiple Cemento-Ossifying Fibroma: A Sign of Hyperparathyroidism-Jaw Tumour Syndrome
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DOI: 10.1155/2023/4664619
Abstract: Hyperparathyroidism-jaw tumour (HPT-JT) syndrome is a rare autosomal dominant disease. It is caused by a gene mutation of the tumour suppressor gene CDC73 that encodes for parafibromin. This syndrome predisposes to a triad occurrence of… read more here.
Keywords: ossifying fibroma; multiple cemento; jaw tumour; hyperparathyroidism jaw ... See more keywords
Genetic Testing in a Patient With Suspected Hyperparathyroidism- Jaw Tumor Syndrome (HPT-JT)
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DOI: 10.1210/jendso/bvab048.396
Abstract: Introduction: Hyperparathyroidism-jaw tumor syndrome (HPT-JT) is a rare autosomal dominant disorder characterized by parathyroid tumors in association with fibro-osseous jaw tumors, uterine tumors and renal lesions. We present a case of suspected HPT-JT. Clinical Case:… read more here.
Keywords: hpt; patient; hyperparathyroidism; genetic testing ... See more keywords