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Mutation of RET codon 768 is associated with the FMTC phenotype.

Authors
  • Boccia, L M
  • Green, J S
  • Joyce, C
  • Eng, C
  • Taylor, S A
  • Mulligan, L M
Type
Published Article
Journal
Clinical genetics
Publication Date
Feb 01, 1997
Volume
51
Issue
2
Pages
81–85
Identifiers
PMID: 9111992
Source
Medline
License
Unknown

Abstract

Multiple endocrine neoplasia type 2A (MEN 2A), type 2B (MEN 2B), and familial medullary thyroid carcinoma (FMTC) are inherited cancer syndromes resulting from mutations in the RET proto-oncogene. Missense mutations of five codons in exons 10 and 11 are found in both MEN 2A and FMTC families, while mutations at codon 768 in exon 13 have been identified in three FMTC families. We report here the results of mutation analysis on a large multi-generation family with multiple cases of medullary thyroid carcinoma (MTC) or C-cell hyperplasia and two individuals with isolated adrenal medullary hyperplasia. A mutation in exon 13, which alters codon 768 from a GAG (Glu) to a GAC (Asp), was found to segregate with the FMTC phenotype in this family but not with the adrenal medullary hyperplasia. These findings suggest that the codon 768 mutation does not predispose to adrenal medullary hyperplasia, but is an accurate predictor of the MTC phenotype in this family.

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