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Wilson Disease is a rare genetic condition where excess copper builds up in the body, mainly affecting the liver and brain. Early diagnosis is crucial, especially in children, as timely treatment can prevent serious complications. In this Part 1 video, Dr. Vibhor Borkar, Pediatric Gastroenterologist, Hepatologist & Liver Transplant Physician, explains: 👉 What is Wilson Disease and how it develops in children 👉 Common symptoms in the liver, brain, and behavior 👉 How doctors diagnose Wilson Disease (blood tests, eye exam, liver tests) 👉 Treatment options – medications, diet, and liver transplant when needed 👉 Importance of family screening and early detection 💡 This video is for parents and caregivers to understand how Wilson Disease affects children, what signs to look out for, and how treatment can help kids live healthier lives. (Wilson disease in children, pediatric liver disease, copper metabolism disorder, Dr Vibhor Borkar Wilson disease, Wilson disease symptoms kids, Wilson disease treatment children, liver transplant kids, pediatric hepatologist Mumbai, genetic liver disease children, Wilson disease awareness) #WilsonDisease #PediatricLiverHealth #DrVibhorBorkar #ChildHealth #LiverCareKids #GeneticDisorder #WilsonDiseaseAwareness #CopperMetabolism #PediatricHepatology