A patient with RET D631Y mutation present with pheochromocytoma

Patients with MEN2A with RET D631Y mutation most commonly present with pheochromocytomas. MTC is a less common part of the syndrome. Therefore, MEN2A caused by the RET D631Y mutation would be a benign nature.

Detalles Bibliográficos
Autor principal: Kim, Jung Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8271257/
https://www.ncbi.nlm.nih.gov/pubmed/34267909
http://dx.doi.org/10.1002/ccr3.4423

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8271257/
https://www.ncbi.nlm.nih.gov/pubmed/34267909
http://dx.doi.org/10.1002/ccr3.4423

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