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Bilateral adrenal pheochromocytoma with a germline L790F mutation in the RET oncogene
About ten percent of pheochromocytomas are associated with familial syndrome. Hereditary pheochromocytoma has characteristics of early onset, multifocality and bilaterality. We experienced a case of 44-year-old man with bilateral pheochromocytoma without evidence of medullary thyroid cancer. Genetic...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Korean Surgical Society
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3294113/ https://ncbi.nlm.nih.gov/pubmed/22403753 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4174/jkss.2012.82.3.185 |
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