Wilsons disease is a genetic disorder in which 1 in 40,000 individuals are affected. It is caused by a recessive gene in which copper metabolism is disordered, so it builds up in the body. This excess of copper can damage the eyes, brain, and liver. A Kayser-Fleisher ring, rust brown ring around the cornea of the eye, is the most characteristic symptom of this disease. Complications usually occur in later years and include: tremors, slurred speech, cirrhosis, clumsiness, and psychological changes. Lifelong treatment is needed for this disease. These are treatments such as Zinc (blocks copper absorption), Penicillamine, Tetrathiomolybdate, and a diet low in copper.
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Wilson's disease is a rare genetic disorder that causes copper to accumulate in the body, leading to damage in the liver, brain, and other organs. Symptoms can include jaundice, tremors, and neurological problems. Treatment involves medications to help remove excess copper and dietary changes to limit copper intake.
Lyme disease is not generally considered to be hereditary, so future children of a father with Lyme disease are not automatically at risk of inheriting the disease from their father. However, they could potentially be exposed to the same environmental factors that can lead to Lyme disease, such as tick bites, so precautions should be taken. It's always best to consult with a healthcare professional for personalized advice.
That will vary from disease to disease and organ to organ.
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Lyme disease is only known as Lyme disease. There are co-infections of Lyme disease that may be mistaken as other names for the disease but they are actually a different infectious disease.For more information about Lyme disease, go to www.lyme.org and http://www.lymediseaseassociation.org
Deficiency disease is night blindness.