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Scandinavian Journal of Gastroenterology Volume 41, 2006 - Issue 4
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CASE REPORT

Morbus Wilson: Case report of a two-year-old child as first manifestation

Anke Beyersdorff Department of Pediatrics, Gastroenterology, Ernst-Moritz-Arndt-Universität Greifswald, GermanyCorrespondence[email protected]
&
Annette Findeisen Department of Pediatrics, Gastroenterology, Ernst-Moritz-Arndt-Universität Greifswald, Germany
Pages 496-497 | Received 14 Jun 2005, Published online: 26 Aug 2009

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Amanda Gomes & George V. Dedoussis. (2016) Geographic distribution of ATP7B mutations in Wilson disease. Annals of Human Biology 43:1, pages 1-8.
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Lian-Jie Lin, Dong-Xu Wang, Nan-Nan Ding, Yan Lin, Yu Jin & Chang-Qing Zheng. (2014) Comprehensive analysis on clinical features of Wilson’s disease: an experience over 28 years with 133 cases. Neurological Research 36:2, pages 157-163.
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Chloe M. Mak & Ching-Wan Lam. (2008) Diagnosis of Wilson's Disease: A Comprehensive Review. Critical Reviews in Clinical Laboratory Sciences 45:3, pages 263-290.
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Articles from other publishers (33)

Maryem Sahli, Abdelali Zrhidri, Youssef El Kadiri, Imane Cherkaoui Jaouad, Toufik Meskini & Abdelaziz Sefiani. (2023) First application of next-generation sequencing in four families with Wilson disease in Morocco. Egyptian Journal of Medical Human Genetics 24:1.
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Irene Maria Ungureanu, Mara Ioana Iesanu, Catalin Boboc, Vlad Cosoreanu, Lorena Vatra, Anna Kadar, Evelina Nicoleta Ignat & Felicia Galos. (2023) Addressing the Challenges in the Diagnosis and Management of Pediatric Wilson’s Disease—Case Report and Literature Review. Medicina 59:4, pages 786.
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Gizem Eşme Kocaman, Didem Ardıçlı & Deniz Yılmaz. (2021) Clinical and laboratory features of children with tremor: a single-center experience. Acta Neurologica Belgica 122:2, pages 479-484.
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Michael L. Schilsky, Eve A. Roberts, Jeff M. Bronstein, Anil Dhawan, James P. Hamilton, Anne Marie Rivard, Mary Kay Washington, Karl Heinz Weiss & Paula C. Zimbrean. (2022) A multidisciplinary approach to the diagnosis and management of Wilson disease: 2022 Practice Guidance on Wilson disease from the American Association for the Study of Liver Diseases. Hepatology Publish Ahead of Print.
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Eun Ju Choe, Jong Won Choi, Minjin Kang, Yong Kang Lee, Han Ho Jeon, Byung Kyu Park, Sun Young Won, Yong Suk Cho, Jeong Hun Seo, Chun Kyon Lee & Jae Bock Chung. (2020) A population-based epidemiology of Wilson’s disease in South Korea between 2010 and 2016. Scientific Reports 10:1.
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Caitlin Mulligan & Jeff M. Bronstein. (2020) Wilson Disease. Neurologic Clinics 38:2, pages 417-432.
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Oksana Ivanivna Kauk, Yevheniia Tarasivna Solovieva, Iryna Oleksandrivna Lapshina & Yuliia Kostiantynivna Remіnyak. (2020) A RARE CLINICAL CASE OF WILSON’S DISEASE MANIFESTATION IN EARLY CHILDHOOD. International Medical Journal:3, pages 49-54.
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Thomas Damgaard Sandahl & Peter Ott. 2019. Wilson Disease. Wilson Disease 85 94 .
Nanda Kerkar & Eve A. Roberts. 2019. Clinical and Translational Perspectives on WILSON DISEASE. Clinical and Translational Perspectives on WILSON DISEASE 179 193 .
F. Woimant, N. Djebrani-Oussedik, C. Collet, N. Girardot & A. Poujois. (2018) The hidden face of Wilson's disease. Revue Neurologique 174:9, pages 589-596.
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Şükrü Güngör, Mukadder Ayşe Selimoğlu, Fatma İlknur Varol & Serdal Güngör. (2018) Pediatric Wilson’s disease: findings in different presentations. A cross-sectional study. Sao Paulo Medical Journal 136:4, pages 304-309.
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E. R. Barantsevich, Yu. P. Kovalchuk, E. V. Melnik, N. V. Shuleshova, V. S. Emanuel & Yu. V. Emanuel. (2018) Neurological manifestations of celiac disease. Dokazatel'naya gastroenterologiya 7:4, pages 87.
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France Woimant, Pascal Chaine & Aurélia Poujois. 2018. Neurometabolic Hereditary Diseases of Adults. Neurometabolic Hereditary Diseases of Adults 147 168 .
N. Cheng, H. Wang, W. Wu, R. Yang, L. Liu, Y. Han, L. Guo, J. Hu, L. Xu, J. Zhao, Y. Han, Q. Liu, K. Li, X. Wang & W. Chen. (2017) Spectrum of ATP7B mutations and genotype-phenotype correlation in large-scale Chinese patients with Wilson Disease . Clinical Genetics 92:1, pages 69-79.
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Eve A. Roberts & Piotr Socha. 2017. Wilson Disease. Wilson Disease 141 156 .
Jung Ah KimHyun Jin KimJin Min ChoSeak Hee OhBeom Hee LeeGu-Hwan KimJin-Ho ChoiKyung Mo KimHan-Wook Yoo. (2015) Diagnostic Value of Ceruloplasmin in the Diagnosis of Pediatric Wilson's Disease. Pediatric Gastroenterology, Hepatology & Nutrition 18:3, pages 187.
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France Woimant & Jean-Marc Trocello. 2014. Neurologic Aspects of Systemic Disease Part II. Neurologic Aspects of Systemic Disease Part II 851 864 .
J.-M. Trocello, E. Broussolle, N. Girardot-Tinant, M. Pelosse, A. Lachaux, C. Lloyd & F. Woimant. (2013) Wilson's disease, 100 years later…. Revue Neurologique 169:12, pages 936-943.
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Alison J. Coffey, Miranda Durkie, Stephen Hague, Kirsten McLay, Jennifer Emmerson, Christine Lo, Stefanie Klaffke, Christopher J. Joyce, Anil Dhawan, Nedim Hadzic, Giorgina Mieli-Vergani, Richard Kirk, K. Elizabeth Allen, David Nicholl, Siew Wong, William Griffiths, Sarah Smithson, Nicola Giffin, Ali Taha, Sally Connolly, Godfrey T. Gillett, Stuart Tanner, Jim Bonham, Basil Sharrack, Aarno Palotie, Magnus Rattray, Ann Dalton & Oliver Bandmann. (2013) A genetic study of Wilson’s disease in the United Kingdom. Brain 136:5, pages 1476-1487.
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F. Woimant, J.-M. Trocello, N. Girardot-Tinant, P. Chaine, R. Sobesky, J.-C. Duclos-Vallée, P. Chappuis, S. El Balkhi & J. Poupon. (2013) Maladie de Wilson. EMC - Neurologie 10:2, pages 1-14.
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Joo Whee Kim. (2013) Genetically confirmed Wilson disease in a 9-month old boy with elevations of aminotransferases. World Journal of Hepatology 5:3, pages 156.
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S. Suresh Kumar, George Kurian, C. E. Eapen & Eve A. Roberts. (2012) Genetics of Wilson’s disease: a clinical perspective. Indian Journal of Gastroenterology 31:6, pages 285-293.
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M.T. Bergoglio, A. Jover Fernández, S. Veses Martín & E. Solá Izquierdo. (2012) Otras enfermedades metabólicas. Medicine - Programa de Formación Médica Continuada Acreditado 11:19, pages 1162-1170.
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Rodolpho Truffa Kleine, Renata Mendes, Renata Pugliese, Irene Miura, Vera Danesi & Gilda Porta. (2012) Wilson's disease: an analysis of 28 Brazilian children. Clinics 67:3, pages 231-235.
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Jeong Kee Seo. (2012) Diagnosis of Wilson Disease in Young Children: Molecular Genetic Testing and a Paradigm Shift from the Laboratory Diagnosis. Pediatric Gastroenterology, Hepatology & Nutrition 15:4, pages 197.
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Andreea M Catana. (2012) Liver transplantation for Wilson disease. World Journal of Hepatology 4:1, pages 5.
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Xin-Hua Li, Yi Lu, Yun Ling, Qing-Chun Fu, Jie Xu, Guo-Qing Zang, Feng Zhou, Yu De-Min, Yue Han, Dong-Hua Zhang, Qi-Ming Gong, Zhi-Meng Lu, Xiao-Fei Kong, Jian-She Wang & Xin-Xin Zhang. (2011) Clinical and molecular characterization of Wilson's disease in China: identification of 14 novel mutations. BMC Medical Genetics 12:1.
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María Dolores Hernández Villén & Sara López Martínez. (2011) Enfermedad de Wilson. Revista del Laboratorio Clínico 4:2, pages 102-111.
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Anne M. Larson. (2008) Acute Liver Failure. Disease-a-Month 54:7, pages 457-485.
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Eve A. Roberts & Michael L. Schilsky. (2008) Diagnosis and treatment of Wilson disease: An update. Hepatology 47:6, pages 2089-2111.
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Harmut H-J Schmidt. (2007) Introducing Single-Nucleotide Polymorphism Markers in the Diagnosis of Wilson Disease. Clinical Chemistry 53:9, pages 1568-1569.
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V. Medici, L. Rossaro & G.C. Sturniolo. (2007) Wilson disease—A practical approach to diagnosis, treatment and follow-up. Digestive and Liver Disease 39:7, pages 601-609.
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E. A. Roberts. 2007. Genetics in Liver Diseases. Genetics in Liver Diseases 78 87 .

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