Related Experiment Video
Updated: Apr 21, 2026

Establishment of a Simple and Effective Rat Model for Intraoperative Parathyroid Gland Imaging
Published on: August 17, 2022
Hyperparathyroidism-Jaw Tumor Syndrome: A Rare Case
Kunal Gupta1, Adlyne Reena Asirvatham2, Shriraam Mahadevan2
1Endocrinology, Diabetes and Metabolism, Sri Ramachandra Institute of Higher Education and Research, Chennai, IND.
Hyperparathyroidism-jaw tumor (HPT-JT) syndrome, a rare genetic disorder, can cause hypercalcemia and jaw tumors. Early diagnosis and surgical intervention are crucial for managing this condition and preventing complications.
Area of Science:
- Endocrinology
- Genetics
- Oncology
Background:
- Hyperparathyroidism-jaw tumor (HPT-JT) syndrome is a rare autosomal dominant disorder.
- It is characterized by primary hyperparathyroidism and ossifying jaw tumors.
More Related Videos
Related Concept Videos
The Parathyroid Glands
Oxyphil cells, whose functions remain elusive, emerge during late puberty, adding a layer of complexity to the parathyroid gland's intricacies. In contrast, principal parathyroid cells undertake a vital role by...
Cushing Syndrome II: Pathophysiology
Graves Disease II: Pathophysiology
Hyperthyroidism II: Pathophysiology
Hormones and Bone Tissue
Hormones That Influence Osteoblasts and/or Maintain the Matrix
Several hormones are necessary for controlling bone growth and maintaining the bone matrix. The pituitary gland secretes growth hormone (GH), which, as its name implies, controls bone growth. This happens in several ways: first, it triggers chondrocyte...
Cushing Syndrome I: Introduction

