MON-509 RET Mutations in the MEN1 Syndrome: Is It an Innocent Bystander?

Introduction MENIN and RET mutations in MEN1 families, are rare, and, when they co-exist either mutation may predominate the clinical picture. We report a family, with both mutations, and, suspect that the RET mutation may not be an innocent bystander. Clinical Cases GM (36M): 2009: Presented with s...

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Detalles Bibliográficos
Autores principales: Rais, Nadeem M, Kumar, Anshul, Jain, Swetha, Mathur, Sandeep Kumar, Scaria, Vinod, Prakash, Savinitha, Joshi, Apoorva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Thyroid
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7207450/
http://dx.doi.org/10.1210/jendso/bvaa046.1622

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