Jaw Tumor

Recent articles about Jaw Tumor

Hyperparathyroidism–jaw Tumor Syndrome: A Report Of Three Large Kindred

[ PUBLICATION ] ... BackgroundHyperparathyroidism–jaw tumor syndrome (HPT–JT) is a rare autosomal disease caused by inactivating germ-line mutations of HRPT2 gene, with subsequent loss of Parafibromin ...
Known for Jaw Tumor | Parathyroid Carcinoma | Parafibromin Expression | Syndrome Hpt

Jaw Tumor: An Uncommon Presenting Manifestation Of Primary Hyperparathyroidism

[ PUBLICATION ] ... “ jaw tumor” and to discuss the clinical implications of a giant cell granuloma vs an ossifying fibroma of the jaw. Material and methods The history, physical examination, laboratory ...
Known for Jaw Tumor | Primary Hyperparathyroidism | Ossifying Fibroma | Genetic Testing

Hyperparathyroidism-Jaw Tumor Syndrome: A Case Report

[ PUBLICATION ] ... hyperparathyroidism-jaw tumor syndrome (HPT-JT). The patient had a family history of primary hyperparathyroidism (PHPT) and uterine fibroma in her mother. The patient presented muscle ...
Known for Jaw Tumor | Primary Hyperparathyroidism Phpt | Hptjt Syndrome | Parathyroid Neoplasms

Recurrence Of Hyperparathyroid Hypercalcemia In A Patient With The Hrpt-2...

[ PUBLICATION ] ... diagnosed jaw tumor and parathyroid carcinoma that presents as a recurrence of hyperparathyroid hypercalcemia. CASE PRESENTATION: A 41-year-old patient who was already diagnosed with a ...
Known for Parathyroid Carcinoma | Jaw Tumor | Cdc73 Gene | Autosomal Dominant

Loss Of Nuclear Expression Of Parafibromin Distinguishes Parathyroid Carcinomas...

[ PUBLICATION ] ... hyperparathyroidism-jaw tumor (HPT-JT) syndrome. Subsequently, somatic mutations have been identified in the majority of sporadic carcinomas. We performed immunohistochemistry
Known for Jaw Tumor | Sporadic Parathyroid | Nuclear Expression | Complete Absence

Hrpt2, Encoding Parafibromin, Is Mutated In Hyperparathyroidism–jaw Tumor Syndrome

[ PUBLICATION ] ... hyperparathyroidism–jaw tumor (HPT–JT) syndrome. A single locus associated with HPT–JT (HRPT2) was previously mapped to chromosomal region 1q25–q32. We refined this region to a critical ...
Known for Jaw Tumor | Encoding Parafibromin | Suppressor Proteins | Gene Hyperparathyroidism

Hyper Parathyroidisim Jaw Tumor Syndrome: A Rare Condition Of Incongruous Features

[ PUBLICATION ] ... Hyperparathyroidism-Jaw Tumor (HPT-JT) syndrome is a rare genetic disorder bearing both a germline and a somatic CDC73 mutation (formerly known as HRPT2), which has been mapped to ...
Known for Jaw Tumor | Ossifying Fibroma | Hptjt Syndrome | Features Hpt

Hyperparathyroidism-Jaw Tumor Syndrome: Results Of Operative Management

[ PUBLICATION ] ... Hyperparathyroidism-jaw tumor syndrome (HPT-JT) is a rare, autosomal-dominant disease secondary to germline-inactivating mutations of the tumor suppressor gene HRPT2/CDC73. The aim of the ...
Known for Jaw Tumor | Parathyroid Disease | Multiglandular Involvement | Retrospective Analysis

Hereditary Hyperparathyroidism-Jaw Tumor Syndrome: The Endocrine Tumor Gene Hrpt2...

[ PUBLICATION ] ... and jaw tumors (HPT-JT) is characterized by inheritance, in an autosomal dominant pattern, of recurrent parathyroid adenomas, fibro-osseous tumors of the mandible and/or maxilla, Wilms ...
Known for Tumor Syndrome | Hereditary Hyperparathyroidism | Chromosome 1 | Loss Heterozygosity

Tumor Suppressor Gene Mutation In A Patient With A History Of...

[ PUBLICATION ] ... Hyperparathyroidism-jaw tumor (HPT-JT) was first observed by Jackson in 1958 in a family who exhibited hyperparathyroidism and recurrent pancreatitis. The author noticed the presence of ...
Known for Jaw Tumor | Parathyroid Carcinoma | Hptjt Syndrome | Osteitis Fibrosa

Recently Asked Questions

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