Wilson's Disease, also known as Hepatolenticular Degeneration is caused by copper accumulation and disrupted copper metabolism caused by the ATP7B gene, inherited in an autosomal recessive manner.

In this informative video, we'll explore the distinct signs of Wilson's Disease, ranging from perplexing neurological symptoms to potential damage to the liver, often indicated by the presence of Kayser-Fleischer Rings – a distinctive marker of excessive copper levels.

Discover the importance of early diagnosis in identifying hepatic dysfunction, and learn about copper chelation therapy using agents like Penicillamine and Trientine to counteract elevated copper levels. We'll also discuss advanced treatments such as Zinc Therapy and the significant option of Liver Transplantation to address severe cases and mitigate potential neurological complications.

Interestingly, Wilson's Disease may also manifest with subtle psychiatric symptoms due to the impact on copper transporters. We'll unravel the complexities of managing this condition and explore the significance of monitoring hepatic copper content in relation to disease progression.

Don't miss this opportunity to unravel the mysteries of Wilson's Disease and gain valuable insights into its diagnosis, treatment, and impact on both the liver and nervous system. Be sure to like, share, and subscribe to stay updated on more captivating explorations of rare medical conditions!

Chapters

00:00 Intro
00:11 Etiology
00:32 Pathophysiology
00:52 Symptoms & Clinical Presentation
01:38 Diagnosis
01:57 Treatment

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