GNAS mutated thyroid carcinoma in a patient with Mc Cune Albright syndrome

Mc Cune-Albright syndrome (MAS) is a rare disorder defined by the triad of polyostotic fibrous dysplasia, “café au lait” skin hyperpigmentation and hyperfunctioning endocrinopathies, such as precocious puberty. MAS is caused by an activating post zygotic somatic mutation of GNAS gene, coding for the...

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Detalles Bibliográficos
Autores principales: Legrand, M.A., Raverot, G., Nicolino, M., Chapurlat, R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7390770/
https://www.ncbi.nlm.nih.gov/pubmed/32760762
http://dx.doi.org/10.1016/j.bonr.2020.100299

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7390770/
https://www.ncbi.nlm.nih.gov/pubmed/32760762
http://dx.doi.org/10.1016/j.bonr.2020.100299

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