Web Analytics Made Easy - Statcounter
Privacy Policy Cookie Policy Terms and Conditions

[HOME PAGE] [STORES] [CLASSICISTRANIERI.COM] [FOTO] [YOUTUBE CHANNEL]


Wilson's disease - MedlinePlus Medical Encyclopedia
Medical Encyclopedia

 

Medical Encyclopedia

Other encyclopedia topics:  A-Ag  Ah-Ap  Aq-Az  B-Bk  Bl-Bz  C-Cg  Ch-Co  Cp-Cz  D-Di  Dj-Dz  E-Ep  Eq-Ez  F  G  H-Hf  Hg-Hz  I-In  Io-Iz  J  K  L-Ln  Lo-Lz  M-Mf  Mg-Mz  N  O  P-Pl  Pm-Pz  Q  R  S-Sh  Si-Sp  Sq-Sz  T-Tn  To-Tz  U  V  W  X  Y  Z  0-9 

Wilson's disease

Contents of this page:

Illustrations

Central nervous system
Central nervous system
Copper urine test
Copper urine test

Alternative Names    Return to top

Hepatolenticular degeneration

Definition    Return to top

Wilson's disease is an inherited disorder in which there is too much copper in the body's tissues. The excess copper damages the liver and nervous system.

Causes    Return to top

Wilson's disease is a rare inherited disorder. If both parents carry an abnormal gene for Wilson's disease, there is a 25% chance in each pregnancy that the child will have the disorder.

Wilson's disease causes the body to take in and keep too much copper. The copper deposits in the liver, brain, kidneys, and the eyes. The deposits of copper cause tissue damage, death of the tissues, and scarring, which causes the affected organs to stop working correctly.

This condition is most common in eastern Europeans, Sicilians, and southern Italians, but may occur in any group. Wilson's disease typically appears in people under 40 years old. In children, the symptoms begin to show by age 4.

Symptoms    Return to top

Exams and Tests    Return to top

A slit-lamp eye examination may show:

A physical examination may show signs of:

Lab tests may include:

If there are liver problems, lab tests may find:

Other tests may include:

The gene responsible for Wilson's disease has been found. It is called ATP7B. DNA testing is available for this gene. However, testing is complicated because different ethnic groups may have different changes (mutations) in this gene.

Treatment    Return to top

The goal of treatment is to reduce the amount of copper in the tissues. This is done by a procedure called chelation -- certain medications can bind to copper and help remove it through the kidneys or gut. Treatment must be lifelong.

The following medications may be used:

Vitamin E supplements may also be used.

Sometimes, medications that chelate copper (especially penicillamine) can affect the function of the brain and nervous system (neurological function). Other medications under investigation may bind copper without affecting neurological function.

A low-copper diet may also be recommended. Foods to avoid include:

You may want to drink distilled water because most tap water flows through copper pipes. Avoid using copper cooking utensils.

Symptoms may be treated with exercise or physical therapy. People who are confused or unable to care for themselves may need special protective measures.

A liver transplant may be considered in cases where the liver is severely damaged by the disease.

Support Groups    Return to top

Wilson's disease support groups can be found at www.wilsonsdisease.org and www.geneticalliance.org.

Outlook (Prognosis)    Return to top

Lifelong treatment is required to control the disorder. The disorder may cause fatal effects, especially loss of liver function and toxic effects of copper on the nervous system. In cases where the disorder is not fatal, symptoms may be disabling.

Possible Complications    Return to top

Liver failure and damage to the central nervous system (brain, spinal cord) are the most common and dangerous effects of the disorder. If not caught and treated early, Wilson's disease is fatal.

When to Contact a Medical Professional    Return to top

Call your health care provider if you have symptoms of Wilson's disease. Call a genetic counselor if you have a history of Wilson's disease in your family and you are planning to have children.

Prevention    Return to top

Genetic counseling is recommended for people with a family history of Wilson's disease.

References    Return to top

Kaler SG. Wilson's Disease. In: Goldman L, Ausiello D, eds. Cecil Medicine. 23rd ed. Philadelphia, Pa: Saunders Elsevier; 2007: chap 230.

Update Date: 8/7/2008

Updated by: Diana Chambers, MS, EdD, Certified Genetics Counselor (ABMG), Charter Member of the ABGC, University of Tennessee, Memphis, TN. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc.

A.D.A.M. Logo

The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed physician should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. Links to other sites are provided for information only -- they do not constitute endorsements of those other sites. Copyright 1997-2009, A.D.A.M., Inc. Any duplication or distribution of the information contained herein is strictly prohibited.


EDIZIONI DI PUBBLICO DOMINIO (HTML)

- La Sacra Bibbia

- Alighieri - La Divina Commedia

RISORSE DAL WEB:

Encyclopaedia Britannica 1911 - PDF

Project Gutenberg: DVD-ROM 2007

Standard E-books

Wikipedia for Schools - ENGLISH

Wikipedia for Schools - FRENCH

Wikipedia for Schools - SPANISH

Wikipedia for Schools - PORTUGUESE

Wikipedia HTML - CATALAN