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Pheochromocytoma in an 8-year-old patient with Multiple Endocrine Neoplasia Type 2A: Implications for Screening
BACKGROUND: Multiple endocrine neoplasia type 2 (MEN2) is an autosomal dominant hereditary cancer syndrome caused by mutations in the RET proto-oncogene. In patients with MEN 2A and 2B the penetrance of pheochromocytoma is variable and childhood pheochromocytoma in the setting of MEN 2 remains rare....
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| Hlavní autoři: | , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2013
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3983847/ https://ncbi.nlm.nih.gov/pubmed/23868299 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jso.23378 |
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