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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Detalles Bibliográficos
Autores principales: Dauth, Nina, Mücke, Victoria T, Mücke, Marcus M, Lange, Christian M, Welker, Martin, Zeuzem, Stefan, Badenhoop, Klaus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2021
Materias:
Unique/Unexpected Symptoms or Presentations of a Disease
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7849456/
https://www.ncbi.nlm.nih.gov/pubmed/33431708
http://dx.doi.org/10.1530/EDM-20-0086

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7849456/
https://www.ncbi.nlm.nih.gov/pubmed/33431708
http://dx.doi.org/10.1530/EDM-20-0086

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