Multiple Endocrine Neoplasia Type 1 with Multiple Leiomyomas Linked to a Novel Mutation in the MEN1 Gene

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominantly inherited syndrome. MEN1 is characterized by the presence of functioning and nonfunctioning tumors or hyperplasia of the pituitary gland, parathyroid glands, and pancreatic islet cells. In addition, MEN1 carriers can have adrenal...

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Detalles Bibliográficos
Autores principales: Choi, Heekyoung, Kim, Sehyun, Moon, Jae-Hoon, Lee, Yoon Hee, Rhee, Yumie, Kang, Eun Seok, Ahn, Chul Woo, Cha, Bong Soo, Lee, Eun Jig, Kim, Kyung Rae, Lee, Hyun Chul, Jeong, Seon Yong, Kim, Hyun Ju, Lim, Sung-Kil
Formato: Texto
Lenguaje:English
Publicado: Yonsei University College of Medicine 2008
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2615294/
https://www.ncbi.nlm.nih.gov/pubmed/18729310
http://dx.doi.org/10.3349/ymj.2008.49.4.655

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