One hundred and seven member family with the rearranged during transfection V804M proto-oncogene mutation presenting with simultaneous medullary and papillary thyroid carcinomas, rare primary hyperparathyroidism, and no pheochromocytomas: Is this a new syndrome-MEN 2C?
作者信息
Shifrin Alexander L, Fay Angela M, Xenachis Cristina Z, Vernick Jerome J
出版信息
Surgery. 2010 Sep;148(3):611-2. doi: 10.1016/j.surg.2010.06.006.
PMID:20719260
Abstract
摘要
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1
One hundred and seven member family with the rearranged during transfection V804M proto-oncogene mutation presenting with simultaneous medullary and papillary thyroid carcinomas, rare primary hyperparathyroidism, and no pheochromocytomas: Is this a new syndrome-MEN 2C?一个有107名成员的家族，其转染期间重排的原癌基因V804M发生突变，同时患有甲状腺髓样癌和乳头状癌、罕见的原发性甲状旁腺功能亢进，且无嗜铬细胞瘤：这是一种新的综合征——MEN 2C吗？
Surgery. 2010 Sep;148(3):611-2. doi: 10.1016/j.surg.2010.06.006.
2
One hundred and seven family members with the rearranged during transfection V804M proto-oncogene mutation presenting with simultaneous medullary and papillary thyroid carcinomas, rare primary hyperparathyroidism, and no pheochromocytomas: is this a new syndrome-MEN 2C?107名携带转染期间重排的V804M原癌基因突变的家庭成员，同时患有甲状腺髓样癌和乳头状甲状腺癌、罕见的原发性甲状旁腺功能亢进，且无嗜铬细胞瘤：这是一种新的综合征——MEN 2C吗？
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3
One hundred and seven family members with the rearranged during transfection V804M proto-oncogene mutation presenting with simultaneous medullary and papillary thyroid carcinomas, rare primary hyperparathyroidism, and no pheochromocytomas: is this a new syndrome--MEN 2C?107名家庭成员存在转染期间重排的V804M原癌基因突变，表现为同时患有甲状腺髓样癌和乳头状癌、罕见的原发性甲状旁腺功能亢进，且无嗜铬细胞瘤：这是一种新的综合征——MEN 2C吗？
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4
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