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http://wilsonsdisease.ca/about-wilson-disease

https://www.genome.gov/27532725/learning-about-wilson-disease/#al-4

https://www.niddk.nih.gov/health-information/liver-disease/wilson-disease

https://en.m.wikipedia.org/wiki/Wilson%27s_disease

https://www.wilsontherapeutics.com/en/section/wilson-disease/

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https://www.wilsontherapeutics.com/en/patient-support/

http://wilsonsdisease.ca/about-wilson-disease

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Wilson's Disease - lecture, etiology, clinical presentation, diagnosis and treatment

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Etiology, clinical presentation, diagnosis and treatment of Wilson's Disease. Animation, Kayser Fleicher ring. Tutorial, ATP7B gene, Apoceruloplasmin, ceruloplasmin, Trientine, penicilamin, and zinc. references: Harrison Internal Medicine 17 edition every content of this video belongs to us

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Patients, physicians and others affected by Wilson Disease talk about life with this rare genetic disease. As a chronic illness, Wilson Disease has a significant, lifelong impact on patients, their families and their healthcare providers. Learn more at wilsontherapeutics.com/en/life-with-wilson-disease.

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Emilee Williams - Fighting Wilson's Disease

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Wilson disease is a genetic disorder that is fatal unless detected and treated before serious illness from copper poisoning develops. Wilson disease affects approximately one in 30,000 people worldwide. The genetic defect causes excessive copper accumulation in the liver or brain. Symptoms typically begin between the ages of 12 and 23.

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Wilson's disease - causes, symptoms, diagnosis, treatment & pathology

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What is Wilson's disease (Wilson disease)? You usually take in more copper than your body needs every day, and any excess is excreted. Subscribe - https://goo.gl/w5aaaV. More videos - https://goo.gl/UhOKiM. Support us on Patreon - https://goo.gl/ZGHEk4. With Wilson's disease, a genetic defect affecting the ATP7B transport protein causes copper to accumulate in the body and damage various tissues and organs.

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Controling copper intake

Removing excess copper

Treating liver problems

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If a family member has been diagnosed

If symptoms are shown, however it may be diagnosed as something else in this way

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Symptoms are categorized into categorys. People dont have all of these at the same time.

1. Liver Disease

2. Neuropsychiatric Symptoms

3. Eyes

4. Kidneys

5. Heart

6. Horomones

Liver Disease

tiredness

portal hypertension

increased bleeding tendency

splenomegaly

ascites

spider anglomata

chronic active hepatitis

cirrhosis

liver cancer

acute liver failure

hemolytic anemia

deranged coagulation

hepatic

Neuropsychiatric

mild cognitive deterioration

clumsiness

changes in behavior

parkinsonism

hand remor

masked facial expressions

slurred speech

atatia

dystonia

seizures

migranes

wing-beating tremor

frontal lobe disorder

subcortical dementia

depression

anxiety disorders

psychosis

Eyes

Kayser-Fleischer Rings

sunflower cataracts

Kidneys

renal tubular acidosis (type 2)

Heart

cardiomyopathy

Hormones

hypoparathyroidism

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Named after Samuel Alexander Kinner Wilson (1912)

Wlison drew from reports by Carl Westphel (1883), William Gowers (1888), and Adolph Strumpell

John Nathaniel Cummings linked copper accumulation in the liver and brain (1948)

The first reported effective treatment was by Derek Denny-Brown with British anti-Lewisite, or Dimercaprol (1951)

This was one of the first therapy available in the field of neurology

The first effective oral medication was penicillamine which was discovered in 1956 by John Walshe

Trientine and tetrathiomolybdate were also tested

Zinc acetate was used by Schouwink and Hoogenraad in 1961 and the 1970's but was later fully developed by Brewer

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Autosomal recessive disease

Causes body to not regulate copper production

Located on chromosome 13