Clinical Features, Treatment, and Surveillance of Hyperparathyroidism-Jaw Tumor Syndrome: An Up-to-Date and Review of the Literature

Hyperparathyroidism-jaw tumor (HPT-JT) syndrome is an autosomal dominant disorder characterized by parathyroid tumors in association with fibro-osseous jaw tumors and uterine and renal lesions. HPT-JT syndrome is caused by germline mutations of the cell division cycle 73 (CDC73) gene that encodes th...

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Detalles Bibliográficos
Autores principales: Torresan, Francesca, Iacobone, Maurizio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6935818/
https://www.ncbi.nlm.nih.gov/pubmed/31929790
http://dx.doi.org/10.1155/2019/1761030

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6935818/
https://www.ncbi.nlm.nih.gov/pubmed/31929790
http://dx.doi.org/10.1155/2019/1761030

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