Late-Onset Medullary Thyroid Cancer in a Patient with a Germline <i>RET</i> Codon C634R Mutation
<b>Background</b>: Multiple endocrine neoplasia type 2A (MEN2A) is a rare, hereditary syndrome resulting from a germline mutation in the <i>RET</i> proto-oncogene and characterized primarily by medullary thyroid cancer (MTC), pheochromocytoma (PHEO), and hyperparathyroidism. Types of <i>RET</i> muta...
I tiakina i:
| Ngā kaituhi matua: | , , , , , , |
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| Hōputu: | Artigo |
| Reo: | Inglês |
| I whakaputaina: |
MDPI AG
2021-08-01
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| Rangatū: | Diagnostics |
| Ngā marau: | |
| Urunga tuihono: | https://www.mdpi.com/2075-4418/11/8/1448 |
| Ngā Tūtohu: |
Kāore He Tūtohu, Me noho koe te mea tuatahi ki te tūtohu i tēnei pūkete!
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