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...
Main Authors: | , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Bioscientifica
2021-01-01
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Series: | Endocrinology, Diabetes & Metabolism Case Reports |
Online Access: | https://edm.bioscientifica.com/view/journals/edm/2021/1/EDM20-0086.xml |