Wilson’s Disease: Public Education

Abstract

Wilson’s Disease is a rare genetic condition that disrupts the body’s ability to eliminate excess copper, leading to its buildup in organs such as the liver, brain, and eyes. This comprehensive article explains the condition in detail, covering its causes, symptoms, types, and genetic inheritance. The article explores the diagnostic process and treatment options, including medications like penicillamine (Cuprimine) and trientine (Syprine) and dietary modifications to manage copper levels. By addressing the challenges of Wilson’s Disease and providing clear, practical advice, this guide supports patients, families, and caregivers in navigating life with the condition.