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Hier erfahren Sie alles über die seltene Erkrankung Kupferstoffwechselkrankeit Morbus Wilson. Ursachen, Symptome, Diagnose und Behandlung.
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RGB
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CMYK
#60B6C6
Fountain Blue
96, 182, 198
189, 47, 58
52, 8, 0, 22
#004E6D
Regal Blue
0, 78, 109
197, 100, 21
100, 28, 0, 57
#FFFFFF
White
255, 255, 255
0, 0, 100
0, 0, 0, 0
Orphalan is a healthcare company that provides information and support for people affected by Wilson disease, a rare inherited disorder that causes harmful copper accumulation in the body. Through its Wilson disease website, the company explains the condition, its causes, symptoms, diagnosis and treatment, helping patients and families better understand the challenges of living with the disease.
The site outlines the importance of lifelong medical treatment and regular monitoring, and offers practical guidance on treatment adherence, everyday life and diet. Its resources include downloadable brochures, including materials for children, and helpful contact information. Orphalan also provides Wilson Care+, a digital therapy-support program for users of Orphalan treatment. The program offers therapy information, treatment insights, support and tools to track progress and share it with a doctor. Additional offerings include the Wilson Academy and educational activities for healthcare professionals, as well as Wilson Talk and a newsletter. Orphalan’s online resources are intended for general education and do not replace professional medical advice, diagnosis or care.
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