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- W2005441606 abstract "Abstract Hirschsprung disease is a congenital condition characterized by a mechanical obstruction caused by inadequate motility in parts of the intestine. This condition can result from mutations in any one of several different genes operating either alone or in combination. Hirschsprung disease has been identified in families with the cancer syndrome multiple endocrine neoplasia type 2a, and it may be the first presentation of the syndrome. Parents of newborns diagnosed with Hirschsprung disease should be counseled on the possible presence of a genetic mutation to the re arranged t ransfection ( RET ) gene on chromosome 10 that predisposes individuals to this hereditary cancer. Risk management strategies can begin early in life to prevent cancer morbidity and mortality. Copyright 2002, Elsevier Science (USA). All rights reserved." @default.
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- W2005441606 date "2002-12-01" @default.
- W2005441606 modified "2023-10-18" @default.
- W2005441606 title "Hirschsprung disease: A component of the familial cancer syndrome multiple endocrine neoplasia type 2a" @default.
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