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Wilson Disease: Mutations in the ATP7B Gene

NEW! Check out our new Holiday survey. Provide input on topics that you would like to see covered: https://www.surveymonkey.de/r/ambossc... The cause of Wilson disease is a mutation in the ATP7B gene, also termed Wilson gene. In most affected individuals, symptoms usually start to appear between 5 and 35 years of age. In its initial stages, liver damage is usually present. As the disease progresses, the central nervous system is involved. Outline: 00:00 - Introduction 02:04 - Pathophysiology 04:29 - Laboratory findings 08:05 - Clinical findings Subscribe to AMBOSS YouTube for the latest clinical examination videos, medical student interviews, study tips and tricks, and live webinars! Free 5-Day Trial: https://go.amboss.com/amboss-YT Instagram:   / amboss_med   Facebook:   / amboss.med   Twitter:   / ambossmed   Blog: https://blog.amboss.com/us #AMBOSSMed #MedicalSchool