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Wilson Disease and Trientine Dihyrodchloride

This website uses cookies. By continuing to use this website you agree to the use of cookies. About cookies. Wilson Disease and Trientine Dihydrochloride. Also known as hepatolenticular degeneration, is a rare inherited autosomal recessive disorder of copper metabolism, resulting in copper toxicity and dysfunction of several organs such as the liver, central nervous system, eyes and kidneys. The disease has a gene frequency of 1 in 90-150 and an incidence of 1 in 30,000. EASL publishes Clinical Practice ...

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Wilson Disease and Trientine Dihyrodchloride | trientine.com Reviews
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This website uses cookies. By continuing to use this website you agree to the use of cookies. About cookies. Wilson Disease and Trientine Dihydrochloride. Also known as hepatolenticular degeneration, is a rare inherited autosomal recessive disorder of copper metabolism, resulting in copper toxicity and dysfunction of several organs such as the liver, central nervous system, eyes and kidneys. The disease has a gene frequency of 1 in 90-150 and an incidence of 1 in 30,000. EASL publishes Clinical Practice ...
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Wilson Disease and Trientine Dihyrodchloride | trientine.com Reviews

https://trientine.com

This website uses cookies. By continuing to use this website you agree to the use of cookies. About cookies. Wilson Disease and Trientine Dihydrochloride. Also known as hepatolenticular degeneration, is a rare inherited autosomal recessive disorder of copper metabolism, resulting in copper toxicity and dysfunction of several organs such as the liver, central nervous system, eyes and kidneys. The disease has a gene frequency of 1 in 90-150 and an incidence of 1 in 30,000. EASL publishes Clinical Practice ...

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1

Wilson's Disease

http://www.trientine.com/wilsons-disease

This website uses cookies. By continuing to use this website you agree to the use of cookies. About cookies. Copper is an essential nutrient which is available from a wide variety of foods such as grains, nuts, meats (liver and kidney), shellfish, legumes (peas and beans), seeds and dark chocolate. Wilson's Disease is caused by mutations in the ATP7B gene. The mutated ATP7B gene prevents the transport protein from functioning properly. Excess copper is therefore not removed from the body and can ...EASL ...

2

Frequently Asked Questions

http://www.trientine.com/frequently-asked-questions

This website uses cookies. By continuing to use this website you agree to the use of cookies. About cookies. What is Trientine capsule for? How does Trientine work? Can I take Trientine with other medicines? Can I take Trientine if I am pregnant? How much Trientine capsules should I take? When should I take my medicine? What should I do if I forget to take my capsules? What should I do if I take too much? Will I have any side effects? How do I store my medicine? Q: What is Trientine capsule for? Pregnant...

3

News Archive

http://www.trientine.com/news

This website uses cookies. By continuing to use this website you agree to the use of cookies. About cookies. EASL publishes Clinical Practice Guidelines for Wilson Disease. The EASL Clinical Practise Guideline: Wilson Disease can be assessed from the Journal of Hepatology 2012 vol.56 pages 671-685. News Stories by Category. News Stories by Year. EASL publishes Clinical Practice Guidelines for Wilson Disease.

4

Scientific Journals

http://www.trientine.com/scientific-journals

This website uses cookies. By continuing to use this website you agree to the use of cookies. About cookies. The following scientific journals are deemed relevant to Wilson Disease. 1 EASL Clinical Practice Guidelines: Wilson’s disease. The EASL Clinical Practise Guideline: Wilson Disease can be assessed from the J ournal of Hepatology. 2012 vol.56 pages 671-685. 2 AASLD practice guidelines: Diagnosis and Treatment of Wilson Disease: An Update. Cho HY et al. Journal of Clinical Pharmacology. 2009...5 Cli...

5

Clinical Presentation

http://www.trientine.com/clinical-manifestations

This website uses cookies. By continuing to use this website you agree to the use of cookies. About cookies. Clinical presentation can vary widely but the most common presentations are with liver disease or neuropsychiatric disturbances1. Asymptomatic patients are most often detected by family screening. Although abnormal copper accumulation begins at birth, the symptoms of WD may not become apparent until late childhood or adolescence, manifesting in the following ways. Clinical findings and biochemical...

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enfermedaddewilson.org enfermedaddewilson.org

Asociación Enfermedad Wilson – Enlaces de interés

http://enfermedaddewilson.org/enlaces-de-interes

Teléfono: 634 582 680. PREGUNTA A LOS EXPERTOS. GUÍAS PARA EL PACIENTE. PREGUNTA A LOS EXPERTOS. GUÍAS PARA EL PACIENTE. Página web de la Federación Española de Enfermedades Raras (F.E.D.E.R.): enfermedades-raras.org. Fundació Per Amor a l’ Art. fundacioperamoralart.es. Trabajo acerca de la Enfermedad de Wilson, escrito por un afectado. http:/ www.edu365.com/aulanet/comsoc/treballsrecerca/treballs 04 05/treb publicats/malatia wilson/wilson.pdf. The European Wilson’s disease registry and network. Nederlan...

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Wilson Disease and Trientine Dihyrodchloride

This website uses cookies. By continuing to use this website you agree to the use of cookies. About cookies. Wilson Disease and Trientine Dihydrochloride. Also known as hepatolenticular degeneration, is a rare inherited autosomal recessive disorder of copper metabolism, resulting in copper toxicity and dysfunction of several organs such as the liver, central nervous system, eyes and kidneys. The disease has a gene frequency of 1 in 90-150 and an incidence of 1 in 30,000. EASL publishes Clinical Practice ...

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