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Presymptomatic DNA screening in families with multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma

✍ Scribed by Andrea Frilling; H. Dralle; C. Eng; F. Raue; C.E. Broelsch

Book ID
117220443
Publisher
Elsevier Science
Year
1995
Tongue
English
Weight
565 KB
Volume
118
Category
Article
ISSN
0039-6060

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Medullary thyroid carcinoma occurs sporadically or as a part of the inherited cancer syndrome multiple endocrine neoplasia (MEN) type 2. The MEN 2 gene has been identified as the RET proto-oncogene on chromosome 10. In MEN 2A, RET mutations are detectable in one of five cysteine codons within exons