Long-term Clinicopathological Features of a Family with Multiple Endocrine Neoplasia Type 2A Caused by C634R RET Gene Mutation

Type 2 multiple endocrine neoplasia (MEN2A) is a variant of hereditary medullary thyroid carcinoma (MTC). MEN2A is characterized by the presence of the following: MTC, hyperparathyroidism, and pheochromocytoma (PHEO). The pathogenesis includes RET proto-oncogene mutation; the most frequently observe...

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Detalles Bibliográficos
Autores principales: Prabhu, Meghana, Shakya, Sunil, Ballal, Sanjana, Shamim, Shamim Ahmed, Bal, Chandrasekhar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Case Series
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6958961/
https://www.ncbi.nlm.nih.gov/pubmed/31949369
http://dx.doi.org/10.4103/ijnm.IJNM_168_19

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6958961/
https://www.ncbi.nlm.nih.gov/pubmed/31949369
http://dx.doi.org/10.4103/ijnm.IJNM_168_19

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