Expressions of Cushing’s syndrome in multiple endocrine neoplasia type 1
Cushing’s syndrome (CS) resulting from endogenous hypercortisolism can be sporadic or can occur in the context of familial disease because of pituitary or extra-pituitary neuroendocrine tumors. Multiple endocrine neoplasia type 1 (MEN1) is unique among familial endocrine tumor syndromes because hype...
Main Author: | William F. Simonds |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2023-06-01
|
Series: | Frontiers in Endocrinology |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fendo.2023.1183297/full |
Similar Items
-
Relapse of the pituitary adenoma with a change of its hormonal activity in a female patient with multiple endocrine neoplasia syndrome type 1
by: L. Ya. Rozhinskaya, et al.
Published: (2018-08-01) -
Multiple endocrine neoplasia type 1 variants and phenocopies
by: E O Mamedova, et al.
Published: (2014-10-01) -
Determinants of Clinical Behavior and Prognosis in Cushing’s Disease: A Quest for Useful Biomarkers
by: Laura C. Hernández-Ramírez
Published: (2022-01-01) -
Management for multiple endocrine neoplasia 1 during pregnancy: clinical and genetic analysis for a pedigree and review of literature
by: Ye Zhiwei, Deng Hongrong, Liu Zhigu, Lin Huimin, Xu Wen, Yao Bin
Published: (2022-03-01) -
Cushing’s Disease as a Result of Two ACTH-Secreting Pituitary Tumors
by: Christine Mathai, MD, et al.
Published: (2021-03-01)