Genetic Analysis of Multiple Endocrine Neoplasia Type 1 (MEN1) Leads to Misdiagnosis of an Extremely Rare Presentation of Intrasellar Cavernous Hemangioma as MEN1

BACKGROUND: Multiple endocrine neoplasia type 1 (MEN1) is a rare inherited disorder characterized by the simultaneous occurrence of endocrine tumors in target tissues (mainly the pituitary, endocrine pancreas, and parathyroid glands). MEN1 is caused by mutations in the MEN1 gene, which functions as...

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Detalles Bibliográficos
Autores principales: Lee, Dong Min, Yu, Seung Hee, Yoon, Hyun Hwa, Lee, Kang Lock, Eom, Young Sil, Lee, Kiyoung, Kim, Byung-Joon, Kim, Yeun Sun, Park, Ie Byung, Kim, Kwang-Won, Lee, Sihoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Endocrine Society 2014
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4091494/
https://www.ncbi.nlm.nih.gov/pubmed/25031887
http://dx.doi.org/10.3803/EnM.2014.29.2.146

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4091494/
https://www.ncbi.nlm.nih.gov/pubmed/25031887
http://dx.doi.org/10.3803/EnM.2014.29.2.146

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