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.
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Видео Wilson Disease: Mutations in the ATP7B Gene канала AMBOSS: Medical Knowledge Distilled
An interactive version of this Chalk Talk episode can be found at:
https://www.amboss.com/us/auditor/wilsondisease
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: https://www.instagram.com/amboss_med/
Facebook: https://www.facebook.com/AMBOSS.Med/
Twitter: https://twitter.com/ambossmed
Blog: https://blog.amboss.com/us
#AMBOSSMed #MedicalSchool
Видео Wilson Disease: Mutations in the ATP7B Gene канала AMBOSS: Medical Knowledge Distilled
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25 октября 2019 г. 3:00:02
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