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

Abstract 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 mon...

وصف كامل

التفاصيل البيبلوغرافية
الحاوية / القاعدة:Orphanet Journal of Rare Diseases
المؤلفون الرئيسيون: Sebastian Zimny, Hélène Bourhis, Sabine Weber, Florian Paul Reiter, Simon Hohenester, Eduard Kraft, Isabelle Mohr, Uta Merle, Karl Heinz Weiss, Gerald Denk
التنسيق: مقال
اللغة:الإنجليزية
منشور في: BMC 2023-05-01
الموضوعات:
Wilson disease
Medical care
Surveillance
الوصول للمادة أونلاين:https://doi.org/10.1186/s13023-023-02731-4

الانترنت

https://doi.org/10.1186/s13023-023-02731-4

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