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Morbus Wilson: Case report of a two-year-old child as first manifestation
Anke Beyersdorff1, Annette Findeisen
1Department of Pediatrics, Gastroenterology, Ernst-Moritz-Arndt-Universität Greifswald, Germany. ab030391@uni-greifswald.de
Abstract:
Morbus Wilson, or Wilson's disease, is a genetic disease of copper metabolism. Usually the disease is detected when the first clinical symptoms appear, generally not before 5 years of age. This case report shows that the disease can be detected much earlier if abnormal laboratory findings in the patient's history prompt further investigations.
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