31. Wilson disease manifestations by neuropsychiatric symptoms: A case report
Main Article Content
Abstract
Wilson’s disease is a disorder of copper metabolism, autosomal recessive inherited, due to ATP7B gene mutation on the long arm of chromosome 13 (13q14.3). Wilson is a rare disease, with a prevalence of 1/30000 to 1/50000 children. With this rate, it is estimated that there are more than 2000 patients with this disease in Vietnam. However, the number of diagnosed patients is many times less than the projected number. In this number, we describe a patient with atypical neuropsychiatric manifestations, with diverse symptoms when diagnosed and treated promptly, responded well to treatment.
Article Details
Keywords
Wilson Disease, Neuropsychiatric symptoms
References
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2. Richard K Gilroy. Wilson Disease: Practice Essentials, Background, Etiology. Accessed August 2, 2022. https://emedicine.medscape.com/article/183456-overview.
3. Cao C, Colangelo T, Dhanekula RK, et al. A Rare Case of Wilson Disease in a 72-Year-Old Patient. ACG Case Rep J. 2019; 6(3): e00024. doi:10.14309/crj.0000000000000024.
4. Guindi M. Wilson disease. Seminars in Diagnostic Pathology. 2019; 36(6): 415-422. doi:10.1053/j.semdp.2019.07.008.
5. Dzieżyc-Jaworska K, Litwin T, Członkowska A. Clinical manifestations of Wilson disease in organs other than the liver and brain. Ann Transl Med. 2019; 7(Suppl 2): S62. doi: 10.21037/atm.2019.03.30
6. Pandey N, John S. Kayser-Fleischer Ring. In: StatPearls. StatPearls Publishing; 2022. Accessed August 2, 2022. http://www.ncbi.nlm.nih.gov/books/NBK459187/.