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Hypopituitarism in Wilson’s disease resolved after copper-chelating therapy
SUMMARY: 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. M...
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| 發表在: | Endocrinol Diabetes Metab Case Rep |
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| Main Authors: | , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Bioscientifica Ltd
2021
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7849456/ https://ncbi.nlm.nih.gov/pubmed/33431708 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1530/EDM-20-0086 |
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