Multiple Cemento-Ossifying Fibroma: A Sign of Hyperparathyroidism-Jaw Tumour Syndrome

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 multiple maxillary or mandibular cemento-ossifying fibroma, par...

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Detalles Bibliográficos
Autores principales: Apandi, Nurul Inaas Mahamad, Basri, Nor Nazaliza, Jalil, Ajura Abdul, Jelon, Md Arad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017210/
https://www.ncbi.nlm.nih.gov/pubmed/36937223
http://dx.doi.org/10.1155/2023/4664619

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017210/
https://www.ncbi.nlm.nih.gov/pubmed/36937223
http://dx.doi.org/10.1155/2023/4664619

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