Wilson's disease is a genetic disorder, which is fatal unless early detected and treated. It is a rare condition, where excess copper builds up in the body causing copper poisoning. Wilson's disease is quite uncommon and affects 1 in 30,000 people. It is named after Dr Samual Wilson, who first described the disorder in 1912.

Copper is a ?trace metal,? which is found in many foods. Some amount of copper intake is necessarily required to remain healthy. Normally, the body automatically gets rid of the excess copper, but a person suffering from Wilson disease is not able to naturally excrete the excess copper. This result in gradual deposition of the excess copper in the vital organs such as the liver, brain, cornea and kidneys ? and if not treated on time, can prove to be potentially fatal.

Generally, the first part of the body to be affected by copper deposits is the liver. In about half of Wilson's disease suffering patients, the liver is the only affected organ. Too much copper in the liver cells (the hepatocytes) is harmful and leads to liver damage.

Excess copper also damages the brain tissue in an area called the lenticular nucleus. Hence, Wilson's disease is also called ?Hepato-lenticular Degeneration?. If left untreated, the damage may become severe and eventually fatal.

The basic underlying deficiency in Wilson disease is not known. It may be related to the body's inability to produce sufficient levels of ceruloplasmin, an enzyme in the fluid portion of the blood that binds to copper and is involved in its transport and regulation. Other scientists believe that reduced production of ceruloplasmin may be the result of a defect in the liver's ability to break down copper. The correlation between reduced ceruloplasmin levels and excessive copper accumulation is not fully understood. In addition, there is also evidence of impaired excretion of copper by the biliary system.

Wilson's disease is quite a rare disease. It is mostly genetically related; therefore, most people inherit it from their parents. It is also quite possible for the mutation to occur spontaneously. One out of 40,000 people inherit Wilson's disease from their parents, and 1/120,000 (one out of four Wilson's disease sufferers) get the disease from a spontaneous mutation.

Although the genetic defect is already present at birth, it takes years for the excess copper to build up to the toxic level where it is fatally damaging.

Symptoms of the disease typically start to develop between the ages of 6 and 20, most commonly in the teenage years. However, you can also develop symptoms in middle age.

The most characteristic sign of this disease is the Kayser-Fleischer ring - a rusty brown ring around the cornea of the eye that can be seen only through an eye exam. Other signs depend on whether the damage occurs in the liver, blood, central nervous system, urinary system, or the musculoskeletal system.

Symptoms of liver disorders often are the first to develop. The toxic effect on the liver cells can cause hepatitis (inflammation of the liver) leading jaundice, abdominal pain and vomiting. If left untreated, damage to liver cells can cause scarring of the liver (cirrhosis). Eventually severe cirrhosis and liver failure develop in untreated cases causing severe problems.

?Physical symptoms such as an odd type of tremor in the arms, slowness of movement, difficulty with speech (dysphagia), writing problems, difficulty swallowing, a wobbly gait, headaches, seizures.

?Psychological symptoms such as depression, mood swings, bizarre and inappropriate behaviour, depression accompanied by suicidal thoughts, neurosis, or psychosis, inability to concentrate. Affected people may become very aggressive and sentimental; and may exhibit a ?change in personality.?

If Wilson's disease is left untreated, the accumulation of copper in the brain can lead to severe problems such as severe muscular weakness, stiffness in the body, and dementia.

Copper may build up in the cornea of the eye. This causes a characteristic feature called Kayser-Fleischer rings - a brownish pigmentation of the cornea. Other features that may develop include anaemia, kidney damage, heart problems, pancreatitis (inflammation of the pancreas), menstrual problems and repeated miscarriage in women, and premature osteoporosis (thinning of the bones).

Wilson's disease is diagnosed with tests that measure the amount of copper in the blood, urine, and liver.

If Wilson's disease is suspected, it is diagnosed by tests such as -

?A blood test to measure ceruloplasmin - a protein that binds copper in the bloodstream.

?A urine test to measure the amount of copper in the urine.

?An examination of the cornea may show the Kayser-Fleischer rings if they have developed.

?A biopsy of the liver

If Wilson's disease gets confirmed in a person, then brothers and sisters should also be tested to see if they have the condition. Siblings of a person with Wilson's disease have a 1/ 4 chance of having the condition.

Cure for Wilson's disease involves a liver transplant, which is performed if necessary to save the person's life. The person will still have the genetic defect, and initial damage to the nervous system will not go, but may improve.

The goal of drug therapy in individuals with Wilson disease is to remove excess copper from the body and prevent ongoing copper accumulation and deposition. Therefore, drug therapy must be continued throughout life. The earlier treatment is started, the better the chance of preventing long-term permanent damage to the liver or brain.