Results 131 to 140 of about 8,287 (164)
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Multiple endocrine neoplasia type 2A: A 25-year review
Journal of Pediatric Surgery, 1999Before 1970, treatment decisions for the thyroid lesions in patients with multiple endocrine neoplasia (MEN) were based on physical findings. For the next 20 years, biological markers assumed a preeminent role, and at present, DNA testing is being used to define the need for therapeutic intervention. This report presents a 25-year review of 22 children
M A, Iler +4 more
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Multiple Endocrine Neoplasia Type 2A in a Kindred With C634Y Mutation
Pediatrics, 2005Multiple endocrine neoplasia type 2A (MEN 2A) is most frequently caused by codon 634 activating mutations. Medullary thyroid carcinoma has occurred before the age of 2, with pheochromocytomas and primary hyperparathyroidism occurring later in childhood.
Malaka B, Jackson +3 more
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Multiple Endocrine Neoplasia Types 1, 2a, and 2b
2003The multiple endocrine neoplasia (MEN) syndromes form a rare distinct group of genetic tumor syndromes inherited in an autosomal dominant fashion. MEN is characterized by the occurrence of tumors involving two or more endocrine glands within an individual.
Christina Orr, Thomas O’Dorisio
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Multiple endocrine neoplasia type 2A
Cancer Genetics and Cytogenetics, 2003Elizabeth McIntyre +5 more
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[Multiple endocrine neoplasia type 2a and 2b].
Ugeskrift for laeger, 1996Multiple endocrine neoplasia type 2a and 2b (MEN 2a and 2b) are rare diseases, inherited as autosomal dominant traits. The neoplasias in MEN 2a are medullary thyroid carcinoma, pheochromocytoma and hyperparathyroidism. In MEN 2b a characteristic phenotype is seen in combination with medullary thyroid carcinoma and pheochromocytoma.
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An interesting case of Multiple Endocrine Neoplasia Type 2A.
La Clinica terapeutica, 2011We report the case of a 37-year-old Chinese man who came with a history of bilateral adrenalectomy and was admitted for recurrent phaeochromocytoma. Further investigations of an incidental finding of persistently raised carcinoembryonic antigen (CEA), fi rst observed four years ago, revealed medullary thyroid carcinoma (MTC).
Chellappah Thambiah, Subashini +4 more
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Multiple endocrine neoplasia type 2A in Chinese families
2012link_to_subscribed_fulltext
Lo, CY +5 more
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Pancreatic Neuroendocrine Neoplasms in Multiple Endocrine Neoplasia Type 1
International Journal of Molecular Sciences, 2021Francesco Tonelli +2 more
exaly