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Wilson Disease: Mutations in the ATP7B Gene

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.

An interactive version of this Chalk Talk episode can be found at:

https://www.amboss.com/us/auditor/wilsondisease

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Видео Wilson Disease: Mutations in the ATP7B Gene канала AMBOSS: Medical Knowledge Distilled
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Информация о видео
25 октября 2019 г. 3:00:02
00:11:21
Яндекс.Метрика