A Familial Case of Multiple Endocrine Neoplasia 2A: From Morphology to Genetic Alterations Penetration in Three Generations of a Family

This paper illustrates a rare syndrome of multiple endocrine neoplasia type 2A (MEN2A) in a family of three generations. In our case, the father, son and one daughter developed phaeochromocytoma (PHEO) and medullary thyroid carcinoma (MTC) over a period of 35 years. Because of the metachronous onset...

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Detalles Bibliográficos
Autores principales: Chen, Lan, Zhang, Jing-Xin, Liu, Dong-Ge, Liu, Hong-Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10000614/
https://www.ncbi.nlm.nih.gov/pubmed/36900098
http://dx.doi.org/10.3390/diagnostics13050955

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10000614/
https://www.ncbi.nlm.nih.gov/pubmed/36900098
http://dx.doi.org/10.3390/diagnostics13050955

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