Abstract
Multiple endocrine neoplasia type 2 (MEN 2) is an autosomal dominant cancer syndrome. Clinical features and diagnostic aspects of this syndrome are reviewed with a focus on progress biochemical screening to genetic analysis of those at risk. The clinical implications resulting from the application of the new methods of molecular biology are discussed.
Publication types
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Drosophila Proteins*
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Humans
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Multiple Endocrine Neoplasia Type 2a / genetics*
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Multiple Endocrine Neoplasia Type 2a / therapy
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Mutation
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Proto-Oncogene Mas
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Proto-Oncogene Proteins / genetics*
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Proto-Oncogene Proteins c-ret
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Receptor Protein-Tyrosine Kinases / genetics*
Substances
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Drosophila Proteins
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MAS1 protein, human
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Proto-Oncogene Mas
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Proto-Oncogene Proteins
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Proto-Oncogene Proteins c-ret
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Receptor Protein-Tyrosine Kinases
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Ret protein, Drosophila