Wilson Disease: Mutations in the ATP7B Gene

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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
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[@anshupal6023]

shortest and the most clear video of wilson disease.....thanks AMBOSS

[@misterkhan9324]

Simply amazing ❤️

[@ezilarasikumaravel4455]

Awesome explanation 😍

[@amirmokhammad5509]

very good explanation!

[@emmyfayed8074]

Great 💪💙

[@captainfalcon7227]

Could someone have these problems and not have Wilson’s disease?