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Should all patients with hyperparathyroidism be screened for a CDC73 mutation?

Primary hyperparathyroidism (PH) is a common endocrine abnormality and may occur as part of a genetic syndrome. Inactivating mutations of the tumour suppressor gene CDC73 have been identified as accounting for a large percentage of hyperparathyroidism-jaw tumour syndrome (HPT-JT) cases and to a less...

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Detalles Bibliográficos
Autores principales: Bachmeier, Caroline, Patel, Chirag, Kanowski, Peter, Sangla, Kunwarjit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5843797/
https://www.ncbi.nlm.nih.gov/pubmed/29535865
http://dx.doi.org/10.1530/EDM-17-0164