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. 2021 Feb 4;71(3):663–674. doi: 10.1007/s12020-021-02633-0

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© The Author(s) 2021

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 3 — Diseases to be considered in cases of prolactinoma. AIP aryl hydrocarbon receptor-interacting protein, AIPneg-FIPA AIP mutation-negative Familial Isolated Pituitary Adenoma (this group does not represent XLAG families), MEN multiple endocrine neoplasia, NF1 neurofibromatosis type 1, 3Pa 3P (phaeochromocytoma, paraganglioma and pituitary adenoma) association, SDH succinate dehydrogenase. *Case reports/further study needed [45]