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         Hepatolenticular Degeneration:     more detail
  1. Studies of protein metabolism in hepatolenticular degeneration (Research report) by Frank L Iber, 1956
  2. Diseases of the Nervous System described for Practitioners and Students with Chapters on the Neurological Complications of Liver Disease and Hepatolenticular Degeneration. by Francis Martin Rouse ; Walshe, John Michael Walshe, 1956-01-01
  3. Wilson's Disease: A Clinician's Guide to Recognition, Diagnosis, and Management by George J. Brewer, 2001-05-31
  4. Orphan Diseases and Orphan Drugs (Fulbright Papers, Proceedings of Colloquia, Vol 3) by I. Herbert Scheinberg, 1986-12
  5. Wilson's Disease by Tjaard Hoogenraad, 1996-07-15
  6. Wilson's Disease for the Patient and Family: A Patient's Guide to Wilson's Disease and Frequently Asked Questions about Copper by George J. Brewer M.D., 2002-04-09
  7. Liver-brain relationships by Ian A Brown, 1957
  8. Die Wilson'sche Krankheit (Westphal-Strümpell'sche Pseudosklerose): Eine Übersicht über die humangenetischen Forschungsergebnisse der Jahre 1967-1977 : Inaugural-Dissertation by Susanne Dworak, 1980
  9. Wilson's disease: Familial presentatin by Ying-tung Kung, 1983

41. Penn State Faculty Research Expertise Database (FRED)
, Hepatocerebral. Degeneration, Hepatolenticular, Degeneration, Neurohepatic.......Faculty Research Expertise Database. hepatolenticular degeneration.
http://fred.hmc.psu.edu/ds/retrieve/fred/meshdescriptor/D006527

42. Liver Information: Hepatolenticular Degeneration Caused By Excessive Deposition
Wilson disease, also referred to as hepatolenticular degeneration, is caused by excessive deposition of copper within the liver, the central nervous system
http://www.livertransplant.org/livernewsletter-wilsondisease.html
Wilson Disease Wilson disease, also referred to as hepatolenticular degeneration, is caused by excessive deposition of copper within the liver, the central nervous system predominately in the basal ganglia and putamen, kidney, placenta and cornea. Patients can present with a wide range of clinical symptoms including movement disorders, speech impediments, psychiatric disorders, renal dysfunction and hemolytic anemia. In the liver, excess copper can cause chronic hepatitis with subsequent cirrhosis and eventual liver failure. Accelerated hepatic injury associated with acute Wilsonian crisis can lead to rapid liver failure and commonly requires liver transplantation. Like hemochromatosis, excessive accumulation of a divalent metal, copper, results in chemical generation of reactive oxygen intermediates causing cellular injury and organ damage. In summary, Wilson disease is an autosomal recessive disease caused by multiple mutations located throughout the WND gene. At this time, the diagnosis of Wilson disease is made by clinical and biochemical evidence of excess copper storage and not by genotyping studies. Haplotype analysis or screening for mutations identified in a Wilson disease patient can be used to identify siblings that may be carriers of the disease before occurrence of the clinical complication of excess copper storage.
Andrew Stolz, M.D.

43. IIDRSI Hepatolenticular Degeneration

http://www.med.univ-rennes1.fr/iidris/index.php?action=contexte&num=1709&mode=mu

44. Wilson's Disease (Hepatolenticular Degeneration) » Clinical And Experimental Op
Wilson s disease (hepatolenticular degeneration). Cockburn DM. © Copyright 2003 Optometrists Association Australia.
http://www.optometrists.asn.au/ceo/backissues/vol70/no1/1647
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Wilson's disease (Hepatolenticular degeneration) Cockburn DM

45. Wilson Disease (hepatolenticular Degeneration)
Wilson disease (hepatolenticular degeneration). References. Search Medline for hepatolenticular degeneration. Related differential diagnosis.
http://www.gentili.net/list4.asp?ID=118

46. HUGO HGM2004 - Poster 278 - Haplotype Analysis For
HGM2004 Poster Abstracts 10. Monogenic Disorders. Poster 278. Haplotype analysis for hepatolenticular degeneration in the Republic of Moldova population.
http://hgm2004.hgu.mrc.ac.uk/Abstracts/Publish/WorkshopPosters/WorkshopPosters10

47. Hepatolenticular Degeneration - General Practice Notebook
hepatolenticular degeneration. Medical search. Wilson s disease is a rare, autosomal recessive disorder first described by KinnearWilson in 1912.
http://www.gpnotebook.co.uk/medwebpage.cfm?ID=1161101336

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49. ORPHANET - Rare Diseases - Orphan Drugs
Printing version, DISEASE Wilson disease, Synonym(s) hepatolenticular degeneration, ICD E83.0, Wilson disease was first described by Dr Wilson in 1912.
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=905

50. Wilson's Disease
DISEASE (hepatolenticular degeneration; Lenticular Degeneration, Progressive; progressive lenticular degeneration; WestphalStruempell pseudosclerosis).
http://www.icongrouponline.com/health/Wilson's_Disease.html
ICON Health Publications
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WILSON'S DISEASE

(Hepatolenticular Degeneration; Lenticular Degeneration, Progressive; progressive lenticular degeneration; Westphal-Struempell pseudosclerosis) Revised and Updated for the Internet Age P A P E R B A C K Paperback Book Paperback Book Order by phone: 800-843-2665 (within USA) 1-201-272-3651 (from outside USA) Paperback Book Shipped in 3 to 5 business days
E B O O K Electronic File * E-Book version sent via e-mail in 2 business days Electronic File *E-Book version sent via e-mail in 2 business days Pages Price $28.95(USD) ISBN Published Synopsis A comprehensive manual for anyone interested in self-directed research on Wilson's disease. Fully referenced with ample Internet listings and glossary. Related Conditions/Synonyms Hepatolenticular Degeneration; Lenticular Degeneration, Progressive; progressive lenticular degeneration; Westphal-Struempell pseudosclerosis Description Table of Contents Introduction Overview Organization Scope Moving Forward PART I: THE ESSENTIALS Chapter 1. The Essentials on Wilson’s Disease: Guidelines

51. Welcome To AJC!
hepatolenticular degeneration. Wilson disease (hepatolenticular degeneration) is a rare inherited disorder, affecting approximately 1 out of 1 million people.
http://www.ajc.com/health/healthfd/shared/health/adam/ency/article/000785.html
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ajc store Gifts Photos/pages Browser tip  Make ajc.com  your homepage: ajc guides Schools Visitors Illustrated Health Encyclopedia Important notice Ency. home Disease W Wilson disease See images Overview Symptoms Treatment ... Prevention Alternative names: Hepatolenticular degeneration Definition: An inherited disorder where there is excessive amounts of copper in the body, which causes a variety of effects including liver disease and damage to the nervous system. Causes and Risks Wilson disease (hepatolenticular degeneration) is a rare inherited disorder, affecting approximately 1 out of 1 million people. If both parents carry an abnormal gene for Wilson disease there is a 25% chance that each of their children will develop the disorder (i.e., Wilson is an autosomal recessive disease). It is most common in eastern Europeans, Sicilians, and southern Italians, but may occur in any group. The disorder most commonly appears in people under 40 years old. In children, the symptoms begin to be expressed by around 4 years old. Wilson disease causes the body to absorb and retain excessive amounts of copper. The copper deposits in the liver, brain, kidneys, and the eyes. The deposits of copper cause tissue damage

52. HerbChina2000.com - Herbal Remedies - Wilson's Disease
the teenage years. Without treatment, the copper poisoning is fatal. SYNONYMS hepatolenticular degeneration. SYMPTOMS Symptoms of
http://www.herbchina2000.com/therapies/PSD.shtml
Home Wilson's disease DESCRIPTION Wilson's disease is a relatively rare genetic disorder, called an 'inborn error of metabolism', that prevents the body from eliminating copper. The build-up of copper damages certain organs including the liver, nervous system, brain, kidneys and eyes. In around half of cases, only the liver is affected. The copper begins to accumulate at birth, but symptoms usually appear during the teenage years. Without treatment, the copper poisoning is fatal. SYNONYMS Hepatolenticular degeneration SYMPTOMS Symptoms of Wilson's disease depend on which structures of the body are affected by copper poisoning, but can include:
  • Enlarged abdomen Abdominal pain Loss of appetite Vomiting of blood Splenomegaly (enlarged spleen) Jaundice (yellowed eyes and skin) Hand tremors Stiffness and reduced movement of the extremities The movement of the body is jerky, slow and difficult to control

53. NGC - Browse
List all 1098 guidelines Digestive System Diseases List all 165 guidelines Liver Diseases - List all 47 guidelines hepatolenticular degeneration - List all 2
http://www.guideline.gov/browse/browsemode.aspx?root=0.0.0.0&path=0.0.0.0.19.10A

54. A Practice Guideline On Wilson Disease.
SCOPE. DISEASE/CONDITION(S). Wilson disease (WD; hepatolenticular degeneration). GUIDELINE CATEGORY. Diagnosis Management Treatment. CLINICAL SPECIALTY.
http://www.guideline.gov/summary/summary.aspx?ss=15&doc_id=3865&nbr=3075

55. MeSH-D Terms Associated To MeSH-C Term Hepatolenticular
MeSHD terms associated to MeSH-C term hepatolenticular degeneration, G2D Home. The number indicates the strength of the association
http://www.bork.embl-heidelberg.de/g2d/c2d.pl?Hepatolenticular_Degeneration:unkn

56. Health Library -
searching the Healthwise Knowledgebase. Also indexed as Copper Overload, hepatolenticular degeneration. Wilson s disease is a genetic
http://yalenewhavenhealth.org/Library/HealthGuide/CAM/topic.asp?hwid=hn-1055001

57. Wilson Disease
Disease Wilson disease, also known as hepatolenticular degeneration, is a rare inherited systemic disorder of copper metabolism. In
http://www.health-nexus.com/wilson_disease1.htm
Health-Nexus.Net Health-Nexus.Org The #1 Health information site
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Wilson Disease
Wilson Disease and Menkes Disease Progress in normal and disordered copper homeostasis, wilson disease, menkes disease, aceruloplasminemia, basic and clinical research. 8th International Conference, April 16 18, 2001.
WE MOVE - Wilson Disease WE MOVE - Wilson Disease ... Wilson disease, also known as hepatolenticular degeneration, is a rare inherited systemic disorder of copper metabolism. In patients with this disease, copper initially ...
Wilson's Disease Association International volunteer organization striving to promote the well-being of patients, their families, and friends.
Wilson disease Wilson disease. Disease type: Copper transport disorder Chromosomes: 13 Aetiology Wilsons...Sarkar B. (1997) Copper transport and its alterations in Menkes and Wilson disease. Biochimica et Biophysica acta. 1360, 3-16. See also: Menkes disease...

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hepatolenticular degeneration. For almost 50 years, the ancient practice of healing and staying healthy through natural remedies
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Herbal Remedies, Alternative Medicine for Men Health, Women Health, Senior Health, Kids Health, Health Information. HerbalGlobal Carries RainTree, Jarrow, Eclectic, Enzymatic, Source Naturals, Planetary Formulas, Twinlab + 800 Brands. Hepatolenticular Degeneration For almost 50 years, the ancient practice of healing and staying healthy through natural remedies was considered backward and inefficient in light of the new science of Pharmacology. It is surprising that North American health practitioners are now rediscovering the herbal traditions in healing. You may be surprised to learn that about half the 'wonder drugs' at the pharmacy are either derived from herbs, or are chemical imitations of substances found in Plants.
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59. Dictionary Definition Of HEPATOLENTICULAR DEGENERATION
Nutritional and Metabolic Diseases Hartnup Disorder OMIM, NCBI (US). hepatolenticular degeneration. About Wilson s Disease - MedStudents (BR). Wilson s Disease Association, International.
http://www.dictionarybarn.com/HEPATOLENTICULAR-DEGENERATION.php
Dictionary definition of HEPATOLENTICULAR DEGENERATION
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Wilson's disease causes the body to absorb and retain copper. The copper deposits in the liver, brain, kidneys and eyes. Complications include dementia and liver failure.
Symptoms include jaundice, vomiting, tremors, weakness and slow stiff movements. Blood tests show serum ceruloplasmin is low. Medications are given to remove the excess copper from the body. Even with life-long treatment, disabling (and life-threatening) side effects are common.
Inheritance: autosomal recessive.
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60. Entrez PubMed
Publication Types Review; Review, Tutorial. MeSH Terms DNA Mutational Analysis; hepatolenticular degeneration*/diagnosis; Hepatolenticular
http://www.comparative-hepatology.com/pubmed/10470603
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Ital J Gastroenterol Hepatol. 1999 Jun-Jul;31(5):416-25. Related Articles, Links
Wilson's disease. Ferenci P. Dept. Internal Medicine IV, Gastroenterology and Hepatology, University of Vienna, Wien, Austria. Publication Types:
  • Review Review, Tutorial

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