Pediatric Wilson disease with early psychiatric manifestations: a case report Journal of Medical Case Reports
Wilson’s disease is an autosomal recessive disorder of copper metabolism that primarily affects theliver and brain, with onset typically in early adulthood. Pediatric presentations are rare, and the
atypical presentation of psychiatric symptoms can delay the diagnosis process in low-resource
settings. Epidemiological data on the disease, particularly in Syria, remain scarce.
تاريخ النشر
24 - يونيو - 2026
أصناف البحث
- علمية
المؤلفون
الكلمات المفتاحية
- pediatric
- neuropsychiatric symptoms
- hepatic
- Wilson disease
