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Article

Different RET gene mutation-induced multiple endocrine neoplasia type 2A in 3 Chinese families.

Medicine - 1 Jan 2017

Liu Qiuli, Tong Dali, Yuan Wenqiang, Liu Gaolei, Yuan Gang, Lan Weihua, Zhang Dianzheng, Zhang Jun, Huang Zaoming, Zhang Yao, Jiang Jun

Abstract excerpt

BACKGROUD: Multiple endocrine neoplasia type 2A (MEN2A) is a condition with inherited autosomal dominant mutations in RET (rearranged during transfection) gene that predisposes the carrier to extremely high risk of medullary thyroid cancer (MTC) and other MEN2A-associated tumors such as parathyroid cancer and/or pheochromocytoma. Little is reported about MEN2A syndrome in the Chinese population. METHODS: All...

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Identifiers

PMID: 28099363
DOI: 10.1097/MD.0000000000005967
PMCID: PMC5279108

Genes

RET

Variants

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