Impact of RET proto-oncogene analysis on the clinical management of multiple endocrine neoplasia type 2

Multiple endocrine neoplasia type 2 (MEN2) is an autosomal dominant disease characterized by the presence of medullary thyroid carcinoma, primary hyperparathyroidism, and pheochromocytoma. Multiple endocrine neoplasia type 2 is still an underdiagnosed, or late-diagnosed condition in many areas of th...

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Hlavní autoři:	Toledo Sergio Pereira de Almeida, Santos Marcelo Augusto Cortina Gonçalves dos, Toledo Rodrigo de Almeida, Lourenço Júnior Delmar Muniz
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Elsevier España 2006-01-01
Edice:	Clinics
Témata:	Endocrine Neoplasia MEN2 RET proto-oncogene Pheochromocytoma Hyperparathyroidism HSCR MTC FMTC
On-line přístup:	http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1807-59322006000100011
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