Medical care of patients with Wilson disease in Germany: a multidisciplinary survey among university centers

BACKGROUND: Wilson disease (WD) is a rare, hereditary disorder of copper metabolism. Due to its variable symptoms and manifestations, diagnosis remains challenging. Affected patients must obtain lifelong medical treatment, as the disease is fatal if untreated. Patients require continuous monitoring,...

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Detalles Bibliográficos
Autores principales: Zimny, Sebastian, Bourhis, Hélène, Weber, Sabine, Reiter, Florian Paul, Hohenester, Simon, Kraft, Eduard, Mohr, Isabelle, Merle, Uta, Weiss, Karl Heinz, Denk, Gerald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10207775/
https://www.ncbi.nlm.nih.gov/pubmed/37226184
http://dx.doi.org/10.1186/s13023-023-02731-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10207775/
https://www.ncbi.nlm.nih.gov/pubmed/37226184
http://dx.doi.org/10.1186/s13023-023-02731-4

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