Hypopituitarism in Wilson’s disease resolved after copper-chelating therapy

Wilson’s disease (WD) is a rare disorder of copper metabolism usually presenting with variable liver damage and neuropsychiatric symptoms. Here we report a 39-year-old Taiwanese female with late manifestation of WD presenting with gonadotroph, thyreotroph and corticotroph hypopituitarism. Molecular...

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Bibliographic Details
Main Authors: Nina Dauth, Victoria T Mücke, Marcus M Mücke, Christian M Lange, Martin Welker, Stefan Zeuzem, Klaus Badenhoop
Format: Article
Language:English
Published: Bioscientifica 2021-01-01
Series:Endocrinology, Diabetes & Metabolism Case Reports
Online Access:https://edm.bioscientifica.com/view/journals/edm/2021/1/EDM20-0086.xml