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Hyper Parathyroidisim Jaw Tumor Syndrome: A Rare Condition of Incongruous Features
BACKGROUND: 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 chromosome 1q25–q31. The association of jaw ossifying fibroma with primary hyperparathyroidisim (PHPT) is ty...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Research and Publications Office of Jimma University
2017
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615003/ https://www.ncbi.nlm.nih.gov/pubmed/29217931 |