Ann Med Med Res | Volume 7, Issue 1 | Case Report | Open Access
Li Y and Wen Y*
Department of Pediatrics, Key Laboratory of Women and Children Diseases, West China Second University Hospital, Sichuan University, Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Ministry of Education, China
Fulltext PDFWilson's Disease (WD) is a rare inherited disorder characterized by impaired hepatic copper metabolism, resulting in copper accumulation and multi-systemic manifestations, but arthritis as an initial manifestation is rare. We report a pediatric case of WD visiting the hospital for arthralgia, and the patient reported gradual improvement with proper therapy.
Li Y, Wen Y. A Pediatric Case of Wilson's Disease Presenting with Arthralgia. Ann Med Medical Res. 2024; 7: 1084..